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Sales Support Coordinator I - Temp to Perm - Billerica, MA
Randstad, Billerica, MA
temporary $ 16.00 - $ 16.00 per hour
Candidate will be a key member of our Process Solutions Sales Coordination team that performs a variety of activities that support our Account Managers and customers. The Sales Coordinator is the dedicated contact for Sales for non technical support such as quotes, sample requests, and general sales reports. In addition to directly supporting the Sales team, they may act as a liaison between Sales, Customer Service, Marketing Management, Product Management, Tradeshow, and Quality Departments as necessary. Essential Duties & Responsibilities: Provide best-in-class sales and customer support via telephone and email Process non-technical customer inquiries: quotations, literature and sample fulfillment, etc. Enter leads from Trade Shows Facilitate service for maintenance and repair of select instrumentation Email customers with product/sales information as requested by Account Manager Run sales reports as requested, including but not limited to Ship History, Item History Support requests for account and contact maintenance in SalesForce.com Support Process Improvement projects Participate in process for annual price increase communication to customers Play a role in non-technical support of Change Notifications Coordinate meeting logistics upon request Working hours: 1st shift Qualifications & Preferences: Bachelor's degree Excellent interpersonal skills in both verbal and written Ability to use multiple computer systems: Oracle, SAP, Lotus Notes, SalesForce.com, and proficient in all Microsoft Office programs including MS Word, MS Excel, and MS Powerpoint Excellent time management & organizational skills Produce work that is well executed, accurate, & attentive to detail and take ownership of all interactions; resourceful and willingness to go above and beyond. Able to meet the challenges of a fast-paced, high-energy environment, while maintaining a strong level of professionalism Temp to Perm potential Benefits Billerica, MA Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 16, 2013
Marketing Assistant
Randstad, Burbank, CA
temporary to hire $ 34,000 - $ 35,000 per year
My client is a major skincare manufacturer in beautiful Burbank CA and is in need of a Marketing Coordinator's is highly capable of performing the duties of the position with a great track record behind them. The responsibilities will include managing day-to-day administrative and marketing functions while supporting the Marketing Department. The essential responsibilities include: - Coordinate multiple assignments and projects assisting with administrative and operational responsibilities of the department - Process and track all vendor invoices for payment. Outsource the printing and marketing jobs to different vendors. - Coordinate and organize meetings, manage calendars, prepare presentations and correspondence. - Interface with all levels of the organization. Route all marketing projects for approval. - Coordinate set up conference calls. - Liaise between department and outside agencies for various meetings/presentations - Arrange departmental meetings and events, executive conference calls, prepare internal and external correspondence. - Maintain department calendar - Coordinate IT and facilities service, arranging all office services and maintenance requests - Help with the creation of all marketing materials. - Manage the parking for entire department - renewal of parking, new parking applications, and physical parking badges. - Set up all janitorial requests for office clean outs, moves. Etc. - Submit all telecom phone request work orders. - Maintain and distribute updated department contact sheets - File invoices Working hours: 8:00AM-5:00PM Qualifications/Requirements --Bachelor's degree --Minimum 1 year of relevant work experience in the field. --Proficient with a PC and Microsoft Word, Excel, and PowerPoint Eligibility Requirements --Must be willing to work in Burbank, CA --Must be willing to submit to a background investigation --Must have unrestricted work authorization to work in the United States Desired Characteristics --Ability to communicate effectively and articulately via phone and email --Proactive, flexible and a team player who is a self starter --Exercise a high level of discretion in handling confidential and sensitive information --Ability to work in a fast paced environment while managing multiple tasks and maintaining a professional attitude --Professional phone manner and in person presence --Effective time management --Maintain strong communication channels across different departments within the organization. --Exceptional writer Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 15, 2013
Validation Test Engineer needed in San Antonio, TX
Randstad, San Antonio, TX
temporary $ 25.00 - $ 35.00 per hour
Position Summary: The Engineer II is responsible for: Test method validation, measurement analysis, and general equipment testing. - Planning, conducting, and reporting on design verification testing within the Global Operations group of a medical device manufacturer - Developing and qualification of test protocols based on design verification and validation requirements - Performing data reduction and preliminary statistical analysis - Providing engineering support for engineers across a broad range of disciplines in the challenging and rewarding medical device industry Primary Duties/Responsibilities: - Function as design verification lead on assigned project teams with accountability for the development, execution, and reporting of verification activities. - Create comprehensive design verification test plans including sample sizes for assigned projects. - Work with manager to develop and execute reliability test plans, as applicable. - Co-ordinate assigned project resources (technicians and equipment) with the objective of assuring data integrity and maximizing test throughput efficiency. - Test protocol development, documentation, and qualification. - Create custom control, user interface, and data collection programs using LabView. - Work with lab technicians to assemble, test, and troubleshoot test setups. - Analyze data from verification and reliability tests for conformance to pre-determined acceptance criteria and prepare formal reports and results summaries. - Assist manager in developing and executing simulated use validation protocols. - Assist engineering team with root cause analysis for problems identified during verification and validation testing. Working hours: First Bachelor Degree in Mechanical Engineering, Biomedical Engineering, or related field. - At least 5 years of experience in an engineering field. - Experience with MS Office applications including: Word, Excel, Project, and Outlook Experience with project management - Experience with ISO 13485 and medical device regulations - Experience with LabView and SolidWorks- - Experience developing and executing reliability test plans - Experience with analogue and digital electronics - Experience troubleshooting, improvising, and work from schematics. - Experience with control systems and process simulation - Experience with solid modeling and engineering drawing creation - Experience in electromechanical system testing and/or design. Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 15, 2013
Phoenix AZ Field Service Engineer - Biotech!!!
Randstad, Billerica, MA
temporary $ 28.00 - $ 28.00 per hour
Successful candidate will be responsible for the installation, repair, and maintenance of water purification systems in the Phoenix AZ area. From time to time the candidate may be asked to travel outside the area to assist his/her colleagues in other territories. The candidate will work with the internal support groups within EMD Millipore Corporation (Lab Water Sales & Service, Logistics, Tech Service) to provide total customer satisfaction. The candidate will make all customer contacts, be responsible for scheduling, and will handle implementation of all services required. The candidate will also be responsible for "marketing" EMD Millipore Corporation's consumables, services , capital upgrades and accessories to all customer contacts. Working hours: 40+ Qualifications The successful candidate will have a minimum of an Associates Degree in electronics/mechanical engineering or equivalent technical or science degree. Experience in the field is a plus but not required. Must be highly organized and have the ability to work independently. A company car is provided so candidate must have an excellent driving record and be willing to travel 5-6 days/month. Long term contract 1yr+ Benefits, Car, Expense Phoenix AZ area Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 15, 2013
Seattle WA Field Service Engineer - Biotech!!!
Randstad, Billerica, MA
temporary $ 28.00 - $ 28.00 per hour
Successful candidate will be responsible for the installation, repair, and maintenance of water purification systems in the Seattle WA area. From time to time the candidate may be asked to travel outside the area to assist his/her colleagues in other territories. The candidate will work with the internal support groups within EMD Millipore Corporation (Lab Water Sales & Service, Logistics, Tech Service) to provide total customer satisfaction. The candidate will make all customer contacts, be responsible for scheduling, and will handle implementation of all services required. The candidate will also be responsible for "marketing" EMD Millipore Corporation's consumables, services , capital upgrades and accessories to all customer contacts. Working hours: 40+ Qualifications The successful candidate will have a minimum of an Associates Degree in electronics/mechanical engineering or equivalent technical or science degree. Experience in the field is a plus but not required. Must be highly organized and have the ability to work independently. A company car is provided so candidate must have an excellent driving record and be willing to travel 5-6 days/month. Long term contract! Benefits, Car, Expense Seattle WA Base Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 15, 2013
Lab Analyst II - St. Charles
Randstad, Saint Charles, MO
temporary $ 16.00 - $ 17.00 per hour
Purpose of the Job: The principal purpose of position is to perform analysis on biological samples on behalf of external Sponsors in accordance with the organisational quality system. Other duties will be necessary in order to ensure that support systems are maintained and internal research projects are performed. Employed as Laboratory Anyalyst, this position is primarily responsible for analysis of samples for CLIA, GxP, or Research. Tasks and Responsibilities: To perform analysis in support of Sponsor assay development, assay transfer, assay validation, and sample analysis studies. Understands and follows all procedures and processes required for work performed under Regulatory Compliance (i.e. GxP, FDA/GLP and GCP, OECD, CLIA, etc.) and attends annual GLP training. To perform analysis in accordance with study plans, analytical procedures and SOPs in order to meet regulatory requirements Documents results of test samples that include calculating the data and repeating analysis. Prepares chemical solutions for use in processing and testing samples following standardized formulas or standard operating procedures. Reads and reviews all new SOP-s and maintains SOP Training file and employee training file. To ensure that all work is performed in compliance with Health and Safety policies and current legislation. To attend internal and external training courses. To assist with the writing of company SOPs and Analytical Procedures To participate in laboratory and other meetings. To participate in internal, Sponsor and regulatory audits. To perform other duties as required by Company management Working hours: 1st Essential --Bachelor-s Degree in a science related field from a four-year college or university; or one to two-years related experience and/or training; or equivalent combination of education and experience. --Ability to read and interpret documents such as safety rules, standard operating procedures, maintenance instructions, and procedure manuals. --Ability to speak effectively before customers and employees. --Ability to perform mathematical calculations such as averages, dilutions, volumes, molarity, and normality. --Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited information is available. --Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. 6 month contract Benefits! Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 15, 2013
Chemistry R&D Tech III
Randstad, Billerica, MA
temporary $ 18.00 - $ 20.00 per hour
Validation Chemistry Laboratory position's primary focus is conducting Extractables studies in a GLP environment and performing chemical analyses for various departments within Millipore. The candidate must be able to follow written Standard Operating Procedures (SOP's) and protocols and design and assemble test systems and apparatus. Also, the candidate will be responsible for the maintenance of the laboratory equipment and instruments. Handling of data and reports and maintenance of laboratory worksheets and equipment calibration records is required. Comprehensive reading and writing of the English language is important. . Handling of various chemicals is necessary. Must be able to read and understand MSDS sheets. Meticulous attention to details and safe work practices is necessary. Must be able work well in a group or individually as duty necessitates. Daily tasks include the use of instruments such as the Total Organic Carbon (TOC) analyzer, Reverse Phase-High Pressure Liquid Chromatography (RP-HPLC) analyzer, viscometer, osmometer, analytical balance, pH meter and Fourier Transform Infrared Spectroscopy (FTIR). Use of computer software including Excel, Word, Origin, Omnic, Lotus Notes and Millenium32. Working hours: 9-5 Bachelors? Degree in Chemistry and have at least 2 years of laboratory experience in the industry. Use of computer software including Excel, Word, Origin, Omnic, Lotus Notes and Millenium32. Hands on working knowledge of HPLC is a requirement GLP experience is a plus! 6 Month Contract Benefits Billerica, MA Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 15, 2013
Sr. Drug Safety Specialist
Randstad, Rockland, MA
temporary
Purpose of the Role: Randstad in partnership with EMD Serono is seeking an experienced Senior Drug Safety Analyst to support the Product Surveillance group in Rockland, MA. The purpose of this role is to provide for the timely initiation, tracking, data entry, and follow up of adverse event reports received for company products according to Federal Regulations and global and local quality documents. Responsibilities: - Understand and adhere to USPS and GDS reporting obligations by initiating and processing adverse event reports within approved timelines as defined in local and global work instructions, SOPs and regulations to meet local and global reporting requirements. - Obtain detailed knowledge of FDA, EMEA and other regulatory authority regulations and apply information to daily work operations. - Receive, prioritize and accurately transfer information from initial and follow-up source documents of serious and non serious adverse event reports to the appropriate fields in ARISg, code adverse events using MedDRA, and accurately advance cases through ARISg workflow within global and local timelines. - Perform Case Initiation duties as assigned. This includes but is not limited to receiving and tracking information regarding potential initial and follow up adverse event reports from all sources, prioritizing and performing searches for duplicates in ARISg prior to the initiation of the case into ARISg, initiating adverse event reports into ARISg, providing reports to assigned staff members for assessment and assuring that cases are returned to case initiation for distribution within defined timelines. - Collect accurate follow up information in a timely manner on non-serious and other adverse event reports. - Communicate with other manufacturers, legal, USMI, USQA, and RA regarding actions to be taken for adverse event reports, as directed. - Understand and utilize labeled information for all EMD Serono marketed products. Working hours: 8:30-5:00 8:30-5:00 Candidates Profile: Overview: Health Care Professional with at least 2 years of specific drug safety experience who will be responsible for: --Data entry including authoring of narratives and quality control of data entry into a validated global safety database --Initial assessment of adverse event reports --Follow up and collection of accurate follow up information for serious, non serious, and other adverse event reports --Adherence to internal and external processes and reporting obligations --Health Care Professional with at least 2 years of specific drug safety experience who will be responsible for: Education/Languages: Degree in a life science or health profession licensure (Nurse, PharmD, Nurse Practitioner, MD, etc.) with a minimum of 4-5 years of experience in Drug Safety or a pharmaceutical company and/or a minimum of 3 to 5 years experience in a healthcare setting. Detailed knowledge of FDA, EMEA and other regulatory authority regulations. English language. Professional Skills & Experience: Good organizational skills with the ability to multi-task and follow projects to completion Experience with database applications (ARISg, Excel, Microsoft Word, etc.) and excellent data entry skills. Personal Skills & Competencies: Ability to effectively communicate with consumers and healthcare professionals. Ability to work effectively as a member of a dynamic team. EMD Serono: Awards & Recognition: June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work! Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 10, 2013
Sr. Drug Safety Specialist
Randstad, Billerica, MA
temporary
Purpose of the Role: Randstad in partnership with EMD Serono is seeking an experienced Senior Drug Safety Analyst to support the Product Surveillance group in Rockland, MA. The purpose of this role is to provide for the timely initiation, tracking, data entry, and follow up of adverse event reports received for company products according to Federal Regulations and global and local quality documents. Responsibilities: - Understand and adhere to USPS and GDS reporting obligations by initiating and processing adverse event reports within approved timelines as defined in local and global work instructions, SOPs and regulations to meet local and global reporting requirements. - Obtain detailed knowledge of FDA, EMEA and other regulatory authority regulations and apply information to daily work operations. - Receive, prioritize and accurately transfer information from initial and follow-up source documents of serious and non serious adverse event reports to the appropriate fields in ARISg, code adverse events using MedDRA, and accurately advance cases through ARISg workflow within global and local timelines. - Perform Case Initiation duties as assigned. This includes but is not limited to receiving and tracking information regarding potential initial and follow up adverse event reports from all sources, prioritizing and performing searches for duplicates in ARISg prior to the initiation of the case into ARISg, initiating adverse event reports into ARISg, providing reports to assigned staff members for assessment and assuring that cases are returned to case initiation for distribution within defined timelines. - Collect accurate follow up information in a timely manner on non-serious and other adverse event reports. - Communicate with other manufacturers, legal, USMI, USQA, and RA regarding actions to be taken for adverse event reports, as directed. - Understand and utilize labeled information for all EMD Serono marketed products. Working hours: 8:30-5:00 Candidates Profile: Overview: Health Care Professional with at least 2 years of specific drug safety experience who will be responsible for: --Data entry including authoring of narratives and quality control of data entry into a validated global safety database --Initial assessment of adverse event reports --Follow up and collection of accurate follow up information for serious, non serious, and other adverse event reports --Adherence to internal and external processes and reporting obligations --Health Care Professional with at least 2 years of specific drug safety experience who will be responsible for: Education/Languages: Degree in a life science or health profession licensure (Nurse, PharmD, Nurse Practitioner, MD, etc.) with a minimum of 4-5 years of experience in Drug Safety or a pharmaceutical company and/or a minimum of 3 to 5 years experience in a healthcare setting. Detailed knowledge of FDA, EMEA and other regulatory authority regulations. English language. Professional Skills & Experience: Good organizational skills with the ability to multi-task and follow projects to completion Experience with database applications (ARISg, Excel, Microsoft Word, etc.) and excellent data entry skills. Personal Skills & Competencies: Ability to effectively communicate with consumers and healthcare professionals. Ability to work effectively as a member of a dynamic team. EMD Serono: Awards & Recognition: June 2009, The Boston Business Journal recognizes EMD Serono as one of the Best Places to Work! Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 10, 2013
Laboratory Tech II - Biotech - Bedford, MA
Randstad, Bedford, MA
temporary
The BioAnalytical Lab, part of the Analytical Technologies group in the Process Solutions Division at EMD Millipore, serves R&D through new method development and analytical support of technology and product development. We are seeking a motivated technician to provide analytical support to R&D teams. Skills needed include working experience with proteins and nucleic acids; familiarity with techniques and instrumentation required for ELISA, protein quantification, chromatography (especially HPLC), electrophoresis, and PCR. We are looking for candidates with protein and analytical backgrounds. The successful candidate will be highly motivated with strong organizational skills, and excellent communication skills. The individual should work well in a collaborative lab environment yet also be capable of working independently to perform, interpret, and troubleshoot biomolecular assays (ELISA, BCA, PicoGreen, SEC-HPLC, q-PCR, SDS-PAGE). The candidate will work under general supervision, with some instruction given for routine work and detailed instructions for new types of work or special projects. Working hours: 9-5 Job Requirements: Qualified candidates will hold a bachelor's degree in a relevant field (biochemistry, chemistry, biology or biophysics) with hands-on laboratory experience in independent scientific research. 6 Month + Contract Benefits Bedford, MA Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 8, 2013
Technical Writer needed in San Antonio, TX 78219
Randstad, San Antonio, TX
temporary $ 14.50 - $ 25.00 per hour
To create/revise as well as initiate/manage change for those labelling items* which fall under the responsibility of Global Product Labeling (GPL). Provide labeling support to numerous functional groups and project teams associated with the new product introduction and global operations. * Including, but not limited to: Guidelines, Instruction for Use, Operations, Repair and Service Manuals, Package Inserts, Product and Package Labels, Quick Reference Guides, Safety Information Sheets, User Guides, Training Information and Marketing Material. Interacting with Engineering, Global Supply Chain, Legal, Marketing, Medical/Safety, Procurement, R&D, Quality & Design Assurance, Regulatory Affairs, Service Engineering, Service Operations Working hours: AM --Average/above average knowledge of graphic design software including (InDesign, Illustrator, Photoshop and Quark). --Average/above average knowledge of writing content in XML. --Average/above average ability to work on tight project schedules. --Average/above average ability to manage multiple priorities and complete tasks in a timely manner. --Average/above average ability to maintain complete confidentiality and discretion in business relationships and exercise sound business judgment. Preferred Qualifications: --Bachelors degree in Technical Writing, Graphic Design, English, Communications and/or other associated discipline. --Previous experience in the healthcare (Pharmaceutical, Medical Device or Biotech) industries. --Microsoft Project, AutoCAD, SolidWorks and/or ProEngineer experience a plus. --Knowledge of a foreign language a plus. Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 6, 2013
DDM Project Manager - Millennium Pharmaceuticals
Randstad, Cambridge, MA
temporary
Drug development and lifecycle management at Millennium are managed through a balanced matrix that uses a central project team model for all programs from late Discovery through commercialization. The position resides in Drug Development Management (DDM). The function is to serve as Project Manager, as a core team member of project teams. Responsibilities include: - Lead cross-functional operational planning for the core team. Align core team members on project goals and deliverables. -Drive development of the integrated development plan that aligns project tactics with the overall project strategy. -Manage daily team operations and ensure completion of activities according to the endorsed development plan and according to the goals. Work with core team members to address issues and risks associated with achieving the deliverables. -Manage and facilitate core team meetings. Ensure appropriate agendas that enable key discussions and decisions within the team. Prepare meeting minutes and follow-up on action items. -Participate in strategic project discussions. Drive scenario discussions and trade-offs (time, cost, quality). Prepare decision trees with clear and agreed to Go/ No Go decision criteria. -Work with the core team to prepare for governance presentations. -Interact with sub-team leaders to align activities of the sub-teams with the needs and strategy of the core team. Participate in sub-team discussions and decisions. This includes non-clinical, clinical, CMC, commercial and regulatory interactions. -Prepare and update key project documentation (monthly reports, timelines, minutes,?) to enable communication of accurate project information to the broader organization. -Facilitate cross-functional conflict and issue resolution. -Lead risk management within the project team. Ensure risks have appropriate mitigation and contingency plans. -Establish and maintain a high performing team and serve as a project advocate within the organization. Working hours: 8:30-5:30pm Duties and Responsibilities: -Serve as a core team members; attend and facilitate core team meetings; prepare and distribute agendas and minutes; follow-up on action items to ensure closure; resolve issues; address risks; ensure alignment between functional lines on deliverables and goals. -Establish, manage and guide project teams to facilitate efficient drug development; outline and monitor development progress; ensure milestones are achieved according to organizational commitments. Understand drug development scenarios and dependencies such that an optimal strategy can be applied to the project. Communicate status and issues to the broader organization through key documents. -Prepare the Integrated Development Plan. Align core team members on components of the plan and ensure the plan is aligned with the project strategy. Work with sub-team leaders to align sub-team activities with the needs and deliverables of the core team. Support maintenance and update of the Integrated Development Plan and other supporting documentation to enable pipeline and milestone decisions. Basic Qualifications: -5-10 years of proven project management experience in a major pharmaceutical and/or biotech company -Minimum of 3 years of oncology experience -Background in a scientific discipline. Graduate degree/ MBA preferred -Strong interpersonal, organization, planning and communication (oral and written) skills Preferred Qualifications: -Graduate degree/MBA preferred. Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 6, 2013
Lab Technician III - Billerica, MA
Randstad, Billerica, MA
temporary
Lab Technician III (B-Shift 230-11pm) The qualified candidate will be responsible for performing microbial retention validation studies on liquid pharmaceutical drug products and/or chemical components with industry standard microorganisms. Responsibilities will include daily preparation and maintenance of a bacterial culture, preliminary qualification testing for retention protocol development, along with microbial retention validation studies. Required to learn and participate in all other laboratory activities, as needed, including but not limited to cleaning and preparation of equipment, autoclave or filter sterilization of test materials, media or solution preparation, routine equipment calibration, equipment maintenance, flush and/or v-max studies, environmental monitoring, laboratory safety and housekeeping, and documentation system maintenance. May be required to write protocols, SOPs and reports. Must work from protocols and departmental SOPs following GMP/GLP guidelines for routine tasks. Required to have the ability and willingness to do non-routine tasks. Must coordinate test activities with other technicians to schedule the use of equipment and obtain testing support. Handling of chemicals and solvents and knowledge of safe handling procedures are necessary. The ideal candidate will be a highly motivated, dynamic, team-oriented person with the ability to coordinate activities and schedule tasks and time with other technicians. Working hours: 2.30PM-11PM REQUIREMENTS: Must have a Bachelor's degree in Biology or Microbiology, or equivalent, plus 1-2 years of experience working in a microbiology laboratory (preferably a pharmaceutical QC microbiology laboratory). Must have the ability to interact and work as a productive team member within the Access Services group. Must have good aseptic technique. Experience working under GMP/GLP regulations and working in a cleanroom is preferable. Experience doing serial dilutions, spread plates and retention testing is helpful. Excellent interpersonal and communication skills, both verbal and written, are required. Experience with word processing and spreadsheet software is necessary. Should possess sound knowledge of fundamentals of Chemistry. 6 Month Contract Benefits Billerica, MA Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 3, 2013
Quality Scientist/Quality Analyst IV
Randstad, North Billerica, MA
temporary
Quality Scientist or Analyst IV level: Purpose Perform testing for stability, raw materials, in-process, and final products in QC Chemistry Laboratory. Analyzes chemical, products, raw materials, in-process materials, release test samples or stability samples. Interprets and evaluates the analyses in terms of accuracy and precision compared against established specifications and recommends and implements corrective action where necessary. Develops, validates, and implements methods. Applies existing techniques and procedures with recommendations and implementation of modification for improved efficiency, or devises and develops new analytical methods and techniques. Performs qualitative tests or quantitative assays on samples using techniques that vary from use of standard analytical equipment to highly modern and automated instrumentation. May also be involved in establishing requirements for the transfer of methodology. Essential Functions Perform routine QC Chemistry testing in accordance with SOPs, safety, and GMP guidelines to support quality release of finished products, raw materials, and various components. Resolves routine problems by utilizing appropriate resources. Execute protocols for procedural and instrumentation validations. Provide problem solving skills to support investigations. Maintain current knowledge of various regulatory requirements and procedures and all internal systems, technology, processes and procedures. Perform paperwork review of Laboratory data to ensure accuracy. Actively promotes safety rules and awareness. Demonstrates good safety practices at all times including the appropriate use of protective equipment. Reports and takes initiative to correct safety & environmental hazards. Actively demonstrates the Lantheus values of accountability, communication, customer commitment, entrepreneurial spirit, integrity, safety and teamwork. Working hours: 8-5 Typical Minimum Skills and Experience and Education -Typically requires 3 + 5 years previous industry experience in the pharmaceutical industry or related GMP environment, or equivalent. -Requires a BA/BS degree in a related science or business discipline or equivalent training and formal experience. Other Requirements -Must complete relevant training as required for compliance with internal and external standards and regulations. Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- May 2, 2013
Senior Business Analyst
Randstad, Saint Louis, MO
temporary
Our client is looking for a Senior Business Analyst to join their emerging field of IT system informatics in defining and delivering breakthrough science in an IT agile software development enterprise. Responsibilities Include: - Interacting successfully as part of a team with software developers, technical architects, test engineers, and support personnel to develop requirements and produce innovative, high quality products. - The successful candidate will develop a thorough and direct understanding of supported business functions, will develop relationships within the technical and business teams, and will drive product development. - This position will work in a liaison relationship with our multi-functional, multi-crop Technology and Commercial organizations, as well as their information technology organization. - Working directly with business partners to define and document requirements, design processes, define limitations, develop and implement solutions. - Coordinating and contributing within all areas of the project life cycle from planning, development, and production implementation through post-implementation support. Partnering with business functions and user networks to translate business requirements into a fully functioning IT design. - Elicit, define, gain consensus on, and manage requirements using techniques such as facilitated workshops, individual interviews, prioritization exercises, and sponsor validation. Required Skills: - Bachelor's degree in Computer Science, Information Systems, Biotechnology, Biology, Agronomy, Breeding or other related degree. - 5+ years of Business Analysis experience or Science related field. Working hours: Monday - Friday; 8am to 4:30pm Desired Skills/Experience: - MBA, MS or PhD in MIS/IS, Agronomy, Plant Breeding, Molecular Breeding, Plant Science, Genetics, Statistics, or Chemistry. - Previous work experience in a biotechnology or agricultural industry. - Knowledge of biotechnology or commercial agricultural seed product management. - Experience working in an Agile environment and as part of a scrum team. - Understanding of relational databases and query tools. - Experience creating and documenting detailed requirements, user stories/specification by example, business processes, fit/gap analysis, and business cases for IT software or systems. - Ability to identify system solutions as well as communicate functional design specifications. - Reconcile input from multiple sources to build and drive the feature development plan for an application or suite of research applications. For immediate consideration qualified candidates should submit a resume to Sara Faris at sara.faris@randstadusa.com Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. [show more]
- April 30, 2013
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terms and conditions
By accessing or using this web site currently located at http://us.randstad.com (the "Web Site") owned by Randstad General Partner (US) LLC on behalf of its subsidiaries and affiliated companies (collectively, "Randstad"), the user of this Web Site and any individual or entity on whose behalf a user accesses or uses the Web Site (collectively, "You" or "Your," as appropriate) agree to be bound by the following Terms and Conditions and to our Privacy Policy. Please read both carefully and often as they are subject to change. Your continued use of the Web Site after the posting of changes to these Terms and Conditions constitutes acceptance of the changes. If You do not agree to these Terms and Conditions, do not use the Web Site.
User Information
When you register for the website, you will be asked to provide Randstad with certain information including, without limitation, a valid email address (your "Information"). In addition to the terms and conditions that may be set forth in any privacy policy on this website, you understand and agree that Randstad may disclose to third parties, on an anonymous basis, certain aggregate information contained in your registration application. Randstad will not disclose to any third party your name, address, email address or telephone number without your prior consent, except to the extent necessary or appropriate to comply with applicable laws or in legal proceedings where such information is relevant. Please see our Privacy Policy for further details regarding your Information.
Registration and Password
You are responsible for maintaining the confidentiality of your information and password. You shall be responsible for all uses of your registration, whether or not authorized by you. You agree to immediately notify Randstad of any unauthorized use of your registration or password.
Modification
Randstad reserves the right to modify the contents of the website or restrict access to the website at any time without notice.
EOE/M/F/D/V.

