Good manufacturing practice Jobs

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Quality Lab Associate - (bachelors degree in science, recent grads) - JC

Cube Hub, Inc.

On-site in Marion, North Carolina, USA

Contract, Third Party

Description: Position Summary 12 hour rotating shift Hours: 7PM - 7AM (Night shift) Conduct sampling and qualitative and quantitative chemical analysis on raw materials, solutions, and components following approved Standard Operating Procedures and test methods in an accurate and timely manner. Job Responsibilities Perform aseptic microbiological and chemical sampling in cleanroom and facility environments Obtain samples from manufacturing environment, ensuring sample integrity and identity

Research Associate II (Infectious Disease)

Zachary Piper Solutions, LLC

On-site in Rockville, Maryland, USA

Full-time

Piper Clinical Solutions is seeking a Research Associate II to support a well-known research organization specializing in infectious disease research in the Rockville, MD area. The Research Associate II will be responsible for performing DNA/RNA extractions and developing novel immunoassays. Responsibilities of the Research Associate II include: Design, generate, and characterize recombinant proteins Perform mammalian cell culture, transient transfections, protein expressions, protein purificat

Microbiology Specialist

Zachary Piper Solutions, LLC

On-site in Durham, North Carolina, USA

Full-time

Piper Companies is seeking a Microbiology Specialist to fill an opportunity with an innovative Pharmaceutical company in Durham, NC. Responsibilities for the Microbiology Specialist Provide testing support to the Microbiology team (Bioburden, Endotoxin, Bioburden, Growth Promotion, Biological Indicators) Maintain laboratory material and reagent inventory Analyze data and complete routine trend reports Assist in laboratory and product failure investigations Document testing in accordance with c

Associate Scientist (Environmental Monitoring)

Zachary Piper Solutions, LLC

On-site in Durham, North Carolina, USA

Full-time

Piper Companies is seeking an Associate Scientist (Environmental Monitoring) to fill an opportunity with an innovative Pharmaceutical company in Durham, NC. Responsibilities for the Associate Scientist (Environmental Monitoring) Provide environmental monitoring support to manufacturing and laboratory groups Support water sampling, and pH water testing Clean steam and compressed gas sample collection Maintain laboratory material and reagent inventory Analyze environmental monitoring data and comp

ECQ Engineer

Zachary Piper Solutions, LLC

On-site in Hopewell Township, New Jersey, USA

Full-time

Piper Companies is currently seeking a ECQ Engineer for an opportunity in Titusville, New Jersey (NJ), to join a global pharmaceutical company. Responsibilities of the ECQ Engineer Maintain, calibrate, qualify and validate equipment used in the production, testing and packaging of pharmaceutical products Develop, execute, and document equipment qualification protocols and test plans in accordance with cGMP regulations and industry standards Commission new laboratory equipment and decommissio

Value Stream/Manufacturing Associate

Arthur Lawrence

On-site in Newark, New Jersey, USA

Contract

Arthur Lawrence is actively looking for a Value Stream/Manufacturing Associate for one of their clients for the contractual opportunity located on-site in Newark, NJ. Must-Have: 1+ years of experience working with cGMP or FDA regulations in a manufacturing/pharmaceutical environment Experience in inventory management and documentation Strong communication skills to communicate effectively with team members and management Knowledge of Good Manufacturing Practice policies, procedures, and guidelin

Senior Validation Engineer

Zachary Piper Solutions, LLC

On-site in Cary, North Carolina, USA

Full-time

Do you have a passion for precision and a keen eye for detail? Do you thrive in fast-paced environments where ensuring quality is part of the culture? If so, then join our growing team as a Validation Engineer and play a vital role in safeguarding the integrity of our pharmaceutical products! In this role, you'll be responsible for ensuring that our manufacturing equipment and processes consistently meet the strictest cGMP standards. You'll leverage your design and field experience to develop a

Senior Scientist

Gables Search Group

On-site in Cranbury, New Jersey, USA

Full-time

Principal/Sr. Scientist, Formulation Development - Job Summary The Principal/Sr. Scientist leads the development of Controlled Release Dosage Forms, from pre-formulation to formulation, aligning with scientific standards and IP strategies. This role entails managing development processes, analyzing data for decision-making, and ensuring compliance with regulatory requirements. Responsibilities: Lead formulation development activities; ensure compliance with SOPs and regulatory standards. Review

MES Engineer

TechDigital Corporation

On-site in Bothell, Washington, USA

Contract

Job Title: MES Engineer Top Skills: A successful candidate will have knowledge and experience with MES technologies. Syncade would be preferable. Similarily: PasX. MS Windows Server and SQL experience required. Knowledge in crystal reports or bartender Experience in C# and VB Script PRINCIPAL OBJECTIVE OF THE POSITION: Provide central support for site integrated manufacturing execution platform. Assure reliable 24/7 operation of integrated manufacturing systems. Develop methods for maintaining

Microbiologist

Zachary Piper Solutions, LLC

On-site in Durham, North Carolina, USA

Full-time

Piper Companies is looking for an Microbiologist to work for a Large Pharmaceutical manufacturer in Durham, NC. Responsibilities for the Microbiologistinclude: Performs analytical testing in the Microbiology Quality Control laboratory Maintain laboratory material and reagent inventory Assist in laboratory and product failure investigations Document testing in accordance with cGMP requirements Qualifications for the Microbiologistinclude: Bachelor of Science in related field is a plus 1+ years o

cGMP Quality Assurance Specialist

Zachary Piper Solutions, LLC

On-site in Everett, Pennsylvania, USA

Full-time

Piper Companies is currently seeking a cGMP Quality Assurance Specialist for an opportunity in Everett, Pennsylvania (PA), to join a pioneering biotechnology company. Responsibilities of the cGMP Quality Assurance Specialist Take a leadership role in quality decisions by supporting change control processes, CAPA systems, deviation processes, nonconforming material processes, customer complaints, supplier approvals, material receiving, internal audit processes and document control Conduct batc

Microbiologist

Judge Group, Inc.

On-site in Leesburg, Virginia, USA

Full-time

Location: Leesburg, VA Salary: $40.00 USD Hourly - $60.00 USD Hourly Description: Our client is currently seeking a Microbiologist for an 8 month + contract. Candidates MUST have gamma sterilization experience Description/Comment: As a Microbiologist you will apply cGLP, cGMP, ANSI, AAMI, ISO, EUMDR, FDA and USP guidelines to the bioburden, cytotoxicity, bacterial endotoxin, and biocompatibility analysis of orthopedic implants and surgical instruments for Leesburg, VA facility. Actively

Analytical Associate II

Apex Systems

On-site in Harleysville, Pennsylvania, USA

Full-time

Job#: 2022111 Job Description: Apex Systems has an exciting opportunity for an Analytical Chemist 2 for one of our Pharmaceutical clients located near Lansdale, PA. The ideal candidate will have 2-4 years of relevant experience. The Chemist will help support the Analytical Laboratory Operations. Primary Responsibilities As an Chemist, you'll join the analytical laboratory as an experienced member of a team of pharmaceutical professionals in support of phase-appropriate drug development and ev

QC Analyst

Apex Systems

On-site in Winchester, Kentucky, USA

Full-time

Job#: 2021242 Job Description: Apex Systems is seeking a QC Analyst near Winchester, KY for a contract to hire opportunity with a growing Biotech Contract Development and Manufacturing Organization (CDMO) with an internationally recognized tradition of quality and service. This role is responsible for Environmental Monitoring sampling, analyzing, and aseptic monitoring and microbiological testing to support Phase I/II GMP manufacturing. The QC Analyst works in a fast-paced environmental supporti

Senior Scientist 1

Gables Search Group

On-site in Cranbury, New Jersey, USA

Full-time

Scientist/Senior Scientist I, Formulation Development - Job Summary The Scientist/Senior Scientist I spearheads pre-formulation, formulation, process development, and scale-up efforts for Controlled Release Dosage Forms. Utilizing a risk-based approach and adhering to cGMP standards, this role encompasses the planning, execution, and documentation of pilot and pivotal batches, ensuring compliance and scientific integrity. Responsibilities: Design and execute development activities for Controlled

CAR-T Logistics Specialist

Johnson & Johnson

On-site in Raritan, New Jersey, USA

Full-time

Description Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a CAR T Warehouse Logistics Specialist located in Raritan, NJ. #CART At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we

Quality Assurance Equipment/Computer System Validation Specialist II

Johnson & Johnson

On-site in Raritan, New Jersey, USA

Full-time

Description Janssen Pharmaceutical, a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Assurance Equipment/Computer System Validation Specialist II-CAR-T Manufacturing. This position will be located in Raritan, NJ. At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to build a world without disease. Redefining lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds a

Scientist, CAR-T Flow Cytometry

Johnson & Johnson

On-site in Malvern, Pennsylvania, USA

Full-time

Description Janssen Research & Development, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for a Scientist, CAR-T Flow Cytometry located in Malvern, PA. At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found. Janssen Research

Senior Development Engineer

Johnson & Johnson

On-site in Cincinnati, Ohio, USA

Full-time

Description Ethicon, a member of Johnson & Johnson's MedTech sector, is currently recruiting for a Senior Development Engineer At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spe

Quality Assurance Associate III

Johnson & Johnson

On-site in Malvern, Pennsylvania, USA

Full-time

Description Janssen Pharmaceuticals, Inc a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality Assurance (QA) Associate located in Malvern, PA! At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are unique