Chief Compliance Officer, Pharmaceutical Industry

**Job Description**Planet Pharma is seeking a skilled GMP Compliance Officer to join our production team. This role requires a strong understanding of GMP regulations and a keen eye for detail.Responsibilities:Evaluate and ensure compliance with cGMP regulations and company policies.Review and approve documentation, including batch production records and...

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 is a global leader in contract development and manufacturing organizations (CDMOs). We are looking for a skilled Engineer II, MS&T to support our manufacturing operations in Maryland.The role involves working as a subject matter expert (SME) for biologic Upstream/Downstream Processes and providing technical support to ensure smooth production....

About the RoleWe are seeking a skilled and detail-oriented professional to fill the position of Batch Records Reviewer. This is an exciting opportunity to join a dynamic team and contribute to the success of our clients in the Pharmaceutical industry.The successful candidate will possess excellent analytical and communication skills, with a strong background...

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...

Job DescriptionWe are seeking a skilled Project Manager to lead our custom automation projects. As a key member of our team, you will be responsible for planning, coordinating, and managing projects from initiation to completion.The ideal candidate will have 2-4 years of project management experience in the medical device or pharmaceutical industries.A...

Job DescriptionVastek Inc is managed by a group of dedicated professionals having rich experience of over years in Healthcare, IT consulting and staffing. We are a certified minority owned, Small business company head quartered out of San Diego, with coverage all across United States, Canada, Mexico, Italy and India.We are looking for a highly motivated...

We are seeking an experienced Project Manager to lead our custom automation projects. As a key member of our team, you will be responsible for planning, coordinating, and managing projects from initiation to completion.Key Responsibilities:Plan, coordinate, and manage projects from initiation to completionEnsure project deliverables meet quality standards,...

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 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,...

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 the development and manufacturing of new treatments for patients worldwide, is seeking an experienced Laboratory Information Management System (LIMS) Administrator to join their team. This role will be responsible for administering accounts, roles, and system functions per global/local LIMS procedures.The ideal candidate will...

About Catalent Inc.Catalent is a global pharmaceutical company dedicated to helping people live better, healthier lives. Our mission is to bring innovative treatments from early development to the market, making a difference in patients' lives worldwide.Job Description:This is a highly specialized role that requires expertise in Laboratory Information...

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...

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...

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...

Key Responsibilities:The Supervisor, QC Analytical will lead analytical testing, investigations, and key deliverables for the Quality Control (QC) group. This role requires expert technical knowledge and the ability to mentor direct reports on basic scientific and regulatory principles.Key Skills and Qualifications:The ideal candidate will have a...

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 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...

Job DescriptionJob Title: Batch Records Reviewer.We are seeking a candidate with genuine experience working with Batch Records. The selected professional will be responsible for reviewing and verifying batch records to ensure accuracy and compliance with regulatory requirements.The ideal candidate should have strong analytical and problem-solving skills,...