GMP Jobs in Pennsylvania

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Supervisor Technical Operations

WuXi AppTec

•

Philadelphia, Pennsylvania, USA

Full-time

Advanced Therapies is a leading global cell and gene therapy contract, testing, development, and manufacturing organization (CTDMO) that is dedicated to advancing the development and commercialization of cell and gene therapies. Our values include innovation, excellence, and collaboration, which are reflected in our mission to accelerate the development and availability of life-saving therapies for patients in need. Working at Advanced Therapies means being part of a dynamic, fast-paced, and
Posted 9 days ago | Updated 8 hours ago

Engineer II, Field Service

Thermo Fisher Scientific

•

Remote or Allentown, Pennsylvania, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc allowed, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting Job Description When you join us at Thermo Fisher Scientific, you'll be part of an inquisitive team that shares your passion for exploration and discover
Posted 33 days ago | Updated moments ago

Engineer I, Field Service

Thermo Fisher Scientific

•

California, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc allowed, Fluctuating Temps hot/cold, Laboratory Setting, Loud Noises (Equipment/Machinery), No contact lens allowed; prescriptive glasses will be provided, Office, Rapid flashing lights, Some degree of PPE (Personal Protective
Posted 14 days ago | Updated moments ago

Field Service Engineer III (IOMS)(MA REMOTE)

Thermo Fisher Scientific

•

Massachusetts, USA

Full-time

Work Schedule First Shift (Days) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Unity Lab Services, a part of Thermo Fisher Scientific, provides integrated solutions, instrument, and enterprise services to our customers. The Engineer Field Service Engineer is responsible for handling all aspects of field service support and customer relationship management including but not limited to: installation, repair, preventative maintenan
Posted 33 days ago | Updated moments ago

Virology Deviation Management Specialist

Zachary Piper Solutions, LLC

•

West Point, Pennsylvania, USA

Full-time

Piper Companies is looking for a Virology Deviation Management Specialist for a leading pharmaceutical manufacturer in West Point, PA. Responsibilities: Conduct deviation management supporting a Virology quality control team Conduct technical writing of deviation investigation results and initiate CAPAs Fully support all aspects of assigned projects and run the business activities, including but not limited to: participate in decision making, leading laboratory investigations, issue ident
Posted 5 days ago | Updated 9 hours ago

Manager 2 - Process Engineering

Motion Recruitment Partners, LLC

•

Horsham, Pennsylvania, USA

Full-time

Principal Process Engineer / Manufacturing Fortune 500 Medical, Biotechnical and Pharmaceutical company is looking to add a Principal Process Engineer to their team in Wilson, NC. This is an initial contract opportunity with perm potential. If you are looking to work for a company that is making a difference for the world you find it. Required Skills & Experience Candidate will need to be commutable distance to Wilson, NC. Role will initially be remote until the Wilson; NC building opens then t
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Posted 18 days ago | Updated 8 hours ago

Virology Deviation Management Specialist

Zachary Piper Solutions, LLC

•

West Point, Pennsylvania, USA

Full-time

Piper Companies is looking for a Virology Deviation Management Specialist for a leading pharmaceutical manufacturer in West Point, PA. Responsibilities: Conduct microbiological testing within investigations to prove root causeRecommend corrective and preventive actions (CAPAs)Conduct deviation OOS investigations related to testing within pharmaceutical manufacturing Qualifications: 2+ years of experience within GMP/FDA regulated environmentFamiliarity with virology Strong background in pharm
Posted 1 day ago | Updated 9 hours ago

Electrical Engineer III

Thermo Fisher Scientific

•

Remote or Marietta, Ohio, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $40 billion. Our Mission is to enable our customers to make the world
Posted 21 days ago | Updated moments ago

Virology Deviation Management Consultant

Zachary Piper Solutions, LLC

•

Lansdale, Pennsylvania, USA

Full-time

Piper Companies is seeking a Deviation Management Consultant to fill an opportunity with a reputable Pharmaceutical company in Lansdale, PA. Responsibilities: Investigate deviations by assessing product impact, identifying root causes, and implementing corrective/preventative actions. Author and update GMP documentation, including SOPs, batch records, validation documents, and change controls. Write quality incident and deviation reports, ensuring thorough analysis and compliance. Collabor
Posted 5 days ago | Updated 9 hours ago

Supplier Quality Specialist

Zachary Piper Solutions, LLC

•

Malvern, Pennsylvania, USA

Full-time

Piper Health and Sciences is actively seeking a Quality Assurance Specialist - Supplier Quality to work for a large global biotechnology company. Responsibilities for Quality Assurance Specialist - Supplier Quality: Oversee the approved supplier list (ASL) including internal and external audits, sending quality agreements, evaluation, and remediation Responsible for writing, reviewing and revising SOPs, CAPAs, deviations, and change controls End-to-end supplier quality including supplier and ven
Posted 1 day ago | Updated 9 hours ago

Supplier Quality Specialist

Zachary Piper Solutions, LLC

•

Plymouth Meeting, Pennsylvania, USA

Full-time

Piper Health and Sciences is actively seeking a Quality Assurance Specialist - Supplier Quality to work for a large global biotechnology company. Responsibilities for Quality Assurance Specialist - Supplier Quality: Oversee the approved supplier list (ASL) including internal and external audits, sending quality agreements, evaluation, and remediation Responsible for writing, reviewing and revising SOPs, CAPAs, deviations, and change controls End-to-end supplier quality including supplier and ve
Posted 1 day ago | Updated 9 hours ago

Deviation Management Specialist

Zachary Piper Solutions, LLC

•

Lansdale, Pennsylvania, USA

Full-time

Piper Companies is seeking a Deviation Management Specialist to fill an opportunity with a reputable Pharmaceutical company in Lansdale, PA. Responsibilities for the Deviation Management Specialist Investigate deviations by assessing product impact, identifying root causes, and implementing corrective/preventative actions. Author and update GMP documentation, including SOPs, batch records, validation documents, and change controls. Write quality incident and deviation reports, ensuring thoro
Posted 5 days ago | Updated 9 hours ago

Quality Control Manager

Zachary Piper Solutions, LLC

•

Wayne, Pennsylvania, USA

Full-time

Piper Companies is seeking a Quality Control Manager to join a reputable Biologics Quality Control Testing company located in Wayne, Pa. Responsibilities of the Quality Control Manager include: Lead projects, collaborate with clients and teams, and ensure expectations are met Oversee testing, manage deviations, and ensure adherence to global regulations Represent the team in audits, address issues, and implement corrective actions Manage assay development, validation, and ongoing compliance
Posted 43 days ago | Updated 9 hours ago

QA Clinical Supplies Specialist

Zachary Piper Solutions, LLC

•

Lansdale, Pennsylvania, USA

Full-time

Piper Companies is seeking a QA Clinical Supplies Specialist to join a major pharmaceutical manufacturing company located in Lansdale, PA. This is a Hybrid role. The QA Clinical Supplies Specialist will ensure the quality, compliance and integrity of clinical trial supplies. Responsibilities of the QA Clinical Supplies Specialist include: Ensure clinical supply materials meet company policies and regulatory standards. Lead projects aimed at improving process performance, including yiel
Posted 43 days ago | Updated 9 hours ago

SAP QM Solution Architect - S4 HANA with EWM.

ArkInfoCubes

•

Exton, Pennsylvania, USA

Contract

Role: SAP QM Solution Architect - S4 HANA with EWM. Location: Extron, PA Experience: 13+ Years Must Have Skills: QM/ Quality Management, S4 HANA, SHOP FLOOR /EWM Summary: The Senior Solution Architect, SAP QM requires in-depth knowledge and experience and is accountable for collaborating with the D&T team in various locations to define, deliver and support IT enabled business solutions for the Quality Management. This role will also help determine business needs and design & deliver technical so
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Posted 4 days ago

Validation Specialist (Onsite) Location: Swiftwater, Pennsylvania

Stellent IT LLC

•

Swiftwater, Pennsylvania, USA

Third Party, Contract

Validation Specialist (Onsite) Location:Swiftwater, Pennsylvania Interview:Phone+Skype Job Description: Ability to write process validation documents and execute Process performance qualification skills required Manager does not want computer validation related roles, Must have manufacturing on the floor experience, collect process samples Must gown up for role and best GMP practices Proficiency in Pi is a plus MANAGER NOTES: Process Validation Proficient in MS Office Strong communication,
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Posted 4 days ago | Updated 1 day ago

Computer System Validation Specialist

SGS Consulting

•

Remote

Contract

Job Title: Computer System Validation (CSV) Specialist Duration: 08 Months + (Possible Extension) Location: Wilmington, DE 19803 (Remote) Schedule: M-F: 08 AM 05 PM Kindly Do not apply if you are not or Permanent Resident of USA. Qualifications: The official position title is Computer System Validation (CSV) specialist to support the Newark manufacturing facility with validation of new and existing computerized systems.This role will primarily support the Newark manufacturing facility but may r
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Posted 11 days ago

C&Q Engineer - (Commissioning & Qualification) || Harrisburg, PA (Onsite)

Stellent IT LLC

•

Harrisburg, Pennsylvania, USA

Contract, Third Party

Position: C&Q Engineer Location: Harrisburg, PA (Onsite) Duration: 12+ month contract Multiple Openings - Standard C&Q profile ideally with 7+ years' experience. More experience the better Job Description :- We are looking for a highly skilled Senior Commissioning & Qualification (C&Q) Engineer to support our Life Sciences projects. The ideal candidate will have extensive experience in qualification and validation activities, ensuring compliance with industry regulations and best practices.
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Posted 32 days ago | Updated 1 day ago

SAP Plant Maintenance (SAP PM)

IT Resonance Inc.

•

Remote

Contract, Third Party

SAP Plant Maintenance (SAP PM) 12 months Remote with travel to onsite (Chicago IL) Must have food & beverage manufacturing or consumer packaged goods industry experience Solid/Strong comm skills compliance with food industry standards (e.g., FDA, GMP, HACCP) Regards Stephen DJA stephen at itresonance dot com
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Posted 17 days ago

Manager, IT

Thermo Fisher Scientific

•

Massachusetts, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description COMPANY: Thermo Fisher Scientific Inc. LOCATION: 168 Third Ave., Waltham, MA 02451 (can work remotely) TITLE: Manager, IT HOURS: Monday to Friday, 8:00 am to 5:00 pm DUTIES: Collaborate with product teams on Software Security tools, vulnerability management, and state-of-the art development practices. Lead security tool evaluations and Proof of Concept to make defensible recommendations on tool, acquisition,
Posted 35 days ago | Updated moments ago