- Catalent Pharma Solutions (Harmans, MD)
- ** Manufacturing Associate II ** **Summary:** _Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the ... therapeutic products including AAV and other viral vector-based therapies and vaccines._ The ** Manufacturing Associate II ** is responsible for supporting the… more
- Cedars-Sinai (Los Angeles, CA)
- …that need our care the most. **Req ID** : 2450 **Working Title** : Research Manufacturing Associate II - Cingolani Lab **Department** : Heart Institute ... **Job Description** JOB SUMMARY: Working under direct supervision, the Manufacturing Associate /Research Associate II performs routine and increasingly… more
- Catalent Pharma Solutions (Princeton, NJ)
- …cell therapy production Catalent Pharma Solutions in Princeton, NJ is hiring a Manufacturing Associate II is responsible for supporting the overall ... of Excellence for cell therapy in Gosselies, Belgium. The CGMP manufacturing facility is equipped with 16...+ High School Diploma with 2+ years of GMP Manufacturing experience required; OR Associate degree in… more
- Endo International (Horsham, PA)
- …are looking for talented individuals to join our team. **Job Description Summary** The Manufacturing Associate II , Upstream Processing works in a hands-on ... with a minimum of 2+ years working in a pharmaceutical/biopharmaceutical cGMP manufacturing environment, OR + BS degree with 1+ years' relevant experience… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** **Key Responsibilities** Associate II , Global External Manufacturing , Small Molecule Drug ... execution of manufacturing campaigns within our global external contract manufacturing network, while ensuring compliance with cGMP , regulatory requirements,… more
- Bristol Myers Squibb (Devens, MA)
- …**Education:** + High school diploma and 2 + years of experience in cGMP bioprocessing manufacturing , cell therapy manufacturing or relevant experience ... engineering discipline and relevant experience is preferred **Experience** + Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy … more
- Catalent Pharma Solutions (Harmans, MD)
- **Specialist II , MTO** **Summary:** _Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. ... EMA and FDA approved facility, at approximately 200,000 sq. ft., houses 10 CGMP manufacturing suites, fill/finish, central services, testing labs, and a… more
- Fujifilm (College Station, TX)
- …innovation, representing a source of pride for the area. **_Summary_** **:** The Manufacturing Technician II work directly with a range of technologies. ... and up to 50 pounds occasionally. + Attendance is mandatory. **_Technician II Minimum Qualifications:_** + Associate 's degree preferably in Biology,… more
- Fujifilm (College Station, TX)
- …+ Work with Quality management to implement quality systems that will enable cGMP manufacturing of pre-clinical to commercial products + Responsible for ... source of pride for the area. **_Summary_** **:** The Manufacturing Compliance Coordinator II assists with the...preferably in Quality Assurance or compliance role; OR + Associate degree and six (6)years' experience in pharmaceutical or… more
- Kelly Services (Durham, NC)
- **Kelly Science has immediate needs for a Manufacturing Associate II in a fast paced biotechnology industry located in Durham NC. This is a contract role ... the possibility of conversion. 1 year of biopharmaceutical or cGMP experienced required for Tech IIs** **Location: Durham NC**...+ Contribute to the buildout and qualification of new manufacturing suites for viral vectors and vaccines + Assist… more
- System One (Mahwah, NJ)
- Title: QC Analytical Associate II Location: Mahwah, NJ area Schedule: Tuesday to Saturday ( 2:30 pm to 11 pm) Type: Contract to Hire Responsibilities: The ... Quality Control Analytical Associate II serves as a support role...written Standard Operating Procedures in accordance to Current Good Manufacturing Practices ( cGMP ) and Good Documentation Practices… more
- BioFire Diagnostics, LLC. (Salt Lake City, UT)
- …Quality System. + Perform repairs involving manual to semi-automated manufacturing and/or packaging equipment. Perform basic routine preventative and scheduled ... as assigned Training and Education + High School diploma or equivalent; Associate 's Degree in a scientific/technical discipline is preferred. Experience + Minimum of… more
- AbbVie (Waco, TX)
- …high-quality solutions, semi-solids, and suspensions in accordance with Good Manufacturing Practices (GMP) and department Standard Operating Procedures (SOP). Job ... in the product formulation process in accordance with current SOP's and cGMP 's. + Accurately complete documents and record production volumes (batches) in compliance… more
- Catalent Pharma Solutions (Kansas City, MO)
- ** Associate Scientist II , Biologics I - Analytical Chemistry** **Position Summary:** Catalent is a global, high-growth, public company and a leading partner for ... the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents,...Pharma Solutions in Kansas City, MO is hiring an Associate Scientist II , Biologics I who is… more
- Fujifilm (College Station, TX)
- …II functions within a team based organization to actively address complex cGMP manufacturing issues. The individual is responsible for analyzing process ... a CMO environment. **External US** **_Essential Functions:_** + Applies scientific and cGMP manufacturing expertise to address issues in the technology transfer… more
- Actalent (Allendale, NJ)
- Job Title: Quality Assurance AssociateJob Description Read, understand, and follow all cGMP and cGTP documentation for Quality System Functions (SOPs, WIs, etc.). ... Maintain cGMP and cGTP compliance for all aspects of pre-clinical,...compliance for all aspects of pre-clinical, clinical, and commercial manufacturing . Perform raw material inspections and raw material release… more
- Catalent Pharma Solutions (Kansas City, MO)
- **Distribution Associate II ** **Position Summary** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the ... Solutions in Kansas City, MO is hiring a Distribution Associate II . This Distribution Associate ...carried out is in compliance with regulatory requirements, good manufacturing practices ( cGMP ) and standard operating procedures… more
- Randstad US (Norwood, MA)
- associate ii , quality control chemistry - 2nd shift, wed-sat. + norwood , massachusetts + posted 5 days ago **job details** summary + $35 - $41.84 per hour + ... 3 to 11 education: Bachelors responsibilities: In this role, you will perform cGMP QC Chemistry testing for QC Chemistry, release, stability and in process samples.… more
- Astellas Pharma (Westborough, MA)
- …per the USP, PhEur, JP or ACS monographs and general chapters in support of manufacturing , based on cGMP 's and internal procedures. Testing includes, but is not ... and technical projects as required. **Quantitative Dimensions:** The QC Analyst II , Raw Materials routinely interact with Manufacturing , Materials Management… more
- Catalent Pharma Solutions (Kansas City, MO)
- …manufacturing practices ( cGMP ) and standard operating procedures (SOPs). The Warehouse Associate II will also support other areas of operation as needed ... **Warehouse Associate II ** **Position Summary:** Catalent Pharma...partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents,… more