talent acquisition specialist salaries in boston, massachusetts

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now!   location: Framingham, Massachusetts job type: Contract salary: $32.00 - 34.39 per hour work hours: 8 to 4 education: Associate   responsibilities: - Operate general manufacturing equipment under close supervision in accordance with current relevant quality standards or standardized procedures and within safety guidelines. - Requires good documentation skills and attention to detail. - Tasks to be completed may include fermentation, protein purification, solvent extractions, tissue culture, preparation of bulk solutions, aseptic fills of buffers, filling and labeling of vials under sterile and non-sterile conditions, routine buffer and media preparation, filtration, vial preparation and sterilization. - Operate general manufacturing equipment in strict accordance with SOPs to complete tasks as noted above as well as large scale bioreactor operations, critical small or large volume sterile fills, and aseptic manipulation of cell cultures. - Operate with minimal supervision complex systems and equipment and optimizes their use in accordance with defined goals. - May participate in plant trials for evaluating process modifications. - Troubleshoot processing problems. - Assist in the implementation of production procedures to optimize manufacturing processes. - May attend research meetings related to the transfer process of new products. - May prepare monthly operating reports for use in the analysis of the performance of the unit. - Participate in authoring complex, explicit documentation for manufacturing operations. - May provide training to new personnel in a specific technical process. - Demonstrated ability in the application of requisite skills and applies additional skills and knowledge acquired through experience to perform the more complex tasks of the position. - Generally receive no instructions on routine assignments while under little or no supervision. - The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Requires physical demands of lifting up to 30 lbs/14 kg to 35 lbs/16 kg.   qualifications: Must Have: - Min 1-3 Years of experience in Pharmaceutical Manufacturing - Experience working with solvents, precipitants, bulk solutions - GDP, GMP - Excellent attendance and team player Nice to Have: - Steam in Place/ SIP - Purification experience a strong plus - Experience with Filter Integrity Testing (FIT): This is a process that uses instrumentation to ensure the filters used in process are integral pre-use and post-use.   skills: SOP, MS-WORD, MS-EXCEL, MS-Powerpoint, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Applications accepted on ongoing basis until filled.

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Cambridge, Massachusetts job type: Contract salary: $30 - 34 per hour work hours: 7 to 3 education: High School   responsibilities: GMP Chemistry is responsible for the execution of nucleotide manufacturing to enable the production of mRNA constructs to be used in clinical and commercial production in a GMP regulated environment. A Manufacturing Associate I execute, under close supervision, all applicable manufacturing unit operations, as directed, following relevant standard operating procedures and cGMP regulations. The work is conducted within a cleanroom environment and typically involves limited physical activity, lifting and standing for periods of time. Follow all relevant GMP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements.Practice safe work habits and adhere to the company's safety procedures and guidelines.Execute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOPs) and work instructions utilizing reader-doer where applicable. Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections. Working in grade C environments and ensuring the manufacturing area is clean and remains in a state of control.Adhere to documented waste handling procedures and respect environmental regulations.Complete training in assigned required learning plan according to the defined timing and the prescribed requalification cadence of gowning and vision, if applicable. Once trained, utilize the manufacturing support systems and equipment as required including, but not limited to, SAP, VEEVA, Delta V, Syncade, LIMS, CMMS.Understands physical and digital systems governing equipment and processes to enable basic troubleshooting.Perform specific unit operations in which they are fully trained.Perform aseptic production of nucleotide constructs using multiple technologies including chemical reaction, TFF operations, chromatography and filtration processes.Filling and dispensing activities to final container closure for finished clinical and commercial nucleotides prior to forward processing.   qualifications: Education: HS DiplomaExperience: STEM degree with 0-1 years' industry experience or an Associates' degree with 2-3 years' industry experience or HS Diploma with 3-5 years' industry experienceDemonstrated ability to learn to gain a strong understanding of GMP regulations.  skills: SOP, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Applications accepted on ongoing basis until filled.

Embrace a thrilling opportunity to work with a leading biotechnology company that is revolutionizing healthcare through groundbreaking mRNA technology. Join a dynamic team of scientists and researchers dedicated to developing life-changing vaccines and therapeutics. At this innovative organization, you'll have the chance to contribute to cutting-edge discoveries and make a meaningful impact on global health. Grow your career in a supportive and collaborative environment, surrounded by passionate individuals driven to make a difference in the world.  salary: $31 - $33 per hourshift: Firstwork hours: 8 AM - 7 PMeducation: BachelorsResponsibilitiesHere’s what you’ll be doing:This role involves actively participating in a collaborative team to execute manufacturing operations using disposable technologies and automation, adhering strictly to cGMPs and standard operating procedures, while demonstrating a keen understanding of bioprocess unit operations and contributing to the production of GMP mRNA-based medicines for human clinical trials. Execute manufacturing operations using disposable technologies, automation, and Manufacturing Execution Systems (MES) to produce mRNAClosely partner with QA peers for rapid disposition of mRNAFollow adherence to current good manufacturing practices, standard operating procedures, and manufacturing documentationEstablish and follow written procedures for the clear and accurate documentation of equipment operation and process instructions, and of process data Here’s what you’ll get: Medical, Dental, Vision, and Disability insuranceAbove market-level compensation starting at $32.00 per hourMultiple shifts availableStart ASAP Skills Manufacturing Qualifications Years of experience: 0 yearsExperience level: Entry Level 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.Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).Applications accepted on ongoing basis until filled.