Pharmaceutical Production Specialist

About Vastek Inc.Vastek Inc is a certified minority-owned small business company specializing in Engineering, Validation, Regulatory, IT, and NON-IT related areas primarily focused on Pharmaceutical / Life Sciences and Medical device companies.Our team of dedicated professionals has rich experience in Healthcare, IT consulting, and staffing, with a strong...

Catalent Inc. offers rewarding opportunities for professionals looking to advance their careers in the pharmaceutical industry.As a GMP Operations Specialist, you will play a crucial role in ensuring the quality and integrity of our products, supporting the development and manufacture of life-enhancing and life-saving treatments.The role involves a...

About Catalent IncCatalent is a global company that partners with the pharmaceutical industry to develop and manufacture new treatments for patients worldwide.Our mission is to help people live better, healthier lives. We have a state-of-the-art CGMP manufacturing facility located on the Harmans/BWI campus, which is close to Washington, DC's I-270 Technology...

Catalent Inc. is a global leader in the development and manufacturing of pharmaceutical products. We are currently seeking a highly skilled Quality Assurance Specialist to join our team.About the Role:The successful candidate will be responsible for providing quality assurance support for GMP manufacturing of master/working cell banks, biological bulk drug...

Catalent Inc. is a leading contract development and manufacturing organization (CDMO) dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers.As a Senior Quality Assurance Specialist at Catalent Inc., you will be responsible for providing quality assurance support for GMP manufacturing of master/working cell banks,...

OverviewCatalent Inc, a global leader in the development and manufacturing of pharmaceuticals, is seeking a Senior Specialist for its Batch Disposition team. Located on the Harmans/BWI campus, our state-of-the-art facility offers an exciting opportunity to work with cutting-edge technology and a talented team of professionals.

The Ideal CandidateWe are looking for a seasoned engineer with 10+ years of experience in GMP/bio-pharma maintenance or engineering, holding a Bachelor of Science in Engineering (Chemical or mechanical preferred). The ideal candidate should possess hands-on expertise in repairing bioprocess equipment, including fermenters, bioreactors, centrifuges,...

Job OverviewWe are seeking a highly skilled Batch Records Specialist to join our team at Vastek Inc. This is an excellent opportunity for a motivated professional to work with a dynamic company that specializes in pharmaceutical and life sciences industries.The successful candidate will be responsible for reviewing and verifying batch records, analyzing...

Job Title: Batch Records ReviewerWe are seeking a candidate with genuine experience working with Batch Records in the Pharma Industry. The ideal candidate will have strong documentation skills and be able to review records efficiently.Key Responsibilities:Reviewing batch records to ensure accuracy and completenessVerifying documentations against established...

Catalent Inc is a leading contract development and manufacturing organization (CDMO) that supports the acceleration of development programs and the launch of new products. We are seeking an experienced Engineer II, MS&T to join our team in Maryland.The role involves supporting GMP manufacturing operations as a subject matter expert (SME) for biologic...

Catalent Inc is a renowned contract development and manufacturing organization (CDMO) dedicated to advancing new medicines from early development to clinical trials and commercialization. We are seeking a highly skilled Engineer II, MS&T to support our Maryland facility.The successful candidate will serve as a subject matter expert (SME) for biologic...

Catalent Inc, a global leader in drug development and delivery, is seeking an experienced Batch Disposition Expert to join our team. This exciting opportunity allows you to utilize your knowledge of pharmaceutical manufacturing practices to ensure compliance with regulatory requirements.In this role, you will be responsible for reviewing GMP documentation...

About the RoleThe Central Services Technician I will be expected to support the execution of GMP manufacturing batch records and ensures necessary supply levels in the manufacturing areas. This role is also responsible for supporting the overall GMP manufacturing process, through the application of broad knowledge of theories and principles utilized to solve...

Central Services TechnicianSalary: $60,000 - $80,000 per annum, depending on experienceJob Description:As a Central Services Technician at Zolon Tech Solutions, Inc., you will play a crucial role in supporting the execution of GMP manufacturing batch records and ensuring necessary supply levels in the manufacturing areas.This position requires broad...

The estimated annual salary for this position in Maryland is $93,280 - $128,260, plus an annual bonus when eligible. This role involves providing Quality Assurance support for GMP documentation of master/working cell banks, bulk drug substance, and finished drug product.

About Us:Catalent Inc. is a growing Contract Development and Manufacturing Organization (CDMO) with an internationally recognized tradition of quality and service. We provide process development and GMP manufacturing services for Phase I/II clinical trials to industry leaders as well as innovative start-ups utilizing novel technologies to produce...

Job Description:Increase your chances of an interview by reading the following overview of this role before making an application.The Manufacturing Technical Specialist will provide support for Manufacturing Management and Associates to meet batch record review/disposition schedule to adhere to lot release dates. The Manufacturing Technical Specialist will...