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Validation
Providing laboratory validation and quality control systems for life science companies is important. By verifying tests and checking on methods, you'll make sure that each test is working properly and that your company continues to succeed. HireLifeScience.com provides validation laboratory technician jobs for people who love the finer details and want to start a new career in life science.
Putting in applications for laboratory technician jobs is a breeze when you put in your application through HireLifeScience.com. Each of these listings features detailed information about the job, letting your know what it takes to work as part of the company's laboratory validation team. Furthermore, you can apply directly to each job from the listing, allowing you to apply to a number of jobs without having to click around. Learn more about lab validation and quality control systems by reading about each job featured here. We offer a wide array of jobs in the United States and other locations across the globe. 

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R&D Analyst

Catalent Pharma Solutions - Indaiatuba, Estado de São Paulo

The Role The responsibilities are: *It should develop appropriate analytical methodologies for raw materials and finished products (content, dissolution and impurities). *It shall elaborate and review analytical methods, prepare and review protocols and reports of Analytical Techniques Validation. Ensure that the methods are validated according to what is requested by the legislation in force ...more

From Catalent Pharma Solutions - 4/25/2018 5:48:56 AM

Associate Director - Engineering

Merck & Co. - West Point, PA

Education Minimum Requirement: • B.S. degree in Engineering or Sciences. • Minimum 8-10 years post-bachelor's degree experience in GMP manufacturing and/or technical support of GMP manufacturing operations (or M.S. degree plus 8 years; PhD degree plus 6 years). Required Experience and Skills**: • Minimum two years of Management or Supervisory experience. • Experience in biologics, vaccin...more

From Merck & Co. - 4/25/2018 5:47:59 AM

Computer Systems Validation Lead

Catalent Pharma Solutions - Kansas City, MO

The role will interface with site Management, Operations, Quality, Metrology and Facilities functions as well as with global Quality and IT functions to ensure the ongoing validated state of GMP systems.  This role will also interface with customers and regulatory authorities in support of ongoing operations and inspections.  Specific Duties, Activities, and Responsibilities: •Act as the Data ...more

From Catalent Pharma Solutions - 4/24/2018 5:53:30 AM

Data Management Associate I

Covance, Inc. a division of LabCorp® - Madison, WI

Education/Qualifications Recommended: Bachelor's degree or equivalent experience. Degree and/or experience in technical writing, document production/publishing, and/or science preferred. Additionally for UK: A minimum of English, Maths, and Science GCSEs, but preferably A level or above. Experience Minimum Required: - Basic knowledge of office software (e.g., Microsoft Office, especial...more

From Covance, Inc. a division of LabCorp® - 4/24/2018 5:52:12 AM

Quality Director

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Education: B.S. in Biology, Chemistry, Engineering or related fields. Master or PhD preferred. AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or ...more

From AstraZeneca Pharmaceuticals - 4/24/2018 5:51:23 AM

Facilities Engineering Technician - RMS Job

Novo Nordisk Inc. - Clayton, NC

CAD, Construction, Diabetes, Drafting, Electrical, Engineer, Engineering, Environmental Health & Safety, Facilities, Healthcare, Industrial Engineer, Maintenance, Manufacturing, Operations, Pharmaceutical, Science, Special Medicine, Technical Support, Technician, Technology

From Novo Nordisk Inc. - 4/23/2018 5:44:38 AM

Scientist

Catalent Pharma Solutions - Morrisville, NC

The Role (daily responsibilities) •Usually works with some supervision, conferring with superior on unusual matters. May be assisted by laboratory technicians/assistants or associate level scientists. Assignments are broad in nature, requiring originality and ingenuity. •Execute analytical methods in a GMP environment •Authors technical documents, such as protocols, test methods, text report...more

From Catalent Pharma Solutions - 4/23/2018 5:44:20 AM

Continued Process Verification Engineer

Catalent Pharma Solutions - Limoges, Région Île-de-France

The Role : You will have two missions: 1) As part of the data integrity regulation, you are implementing data governance in the pharmaceutical quality system to meet regulatory expectations. You will assist the different departments of the site to optimize the manual GMP data processing systems. In addition, you apply ALCOA best practices in data management throughout the entire data lifecycle. ...more

From Catalent Pharma Solutions - 4/23/2018 5:44:20 AM

QA Technical Specialist - (Louisville, KY)

AstraZeneca Pharmaceuticals - Shepherdsville, KY

Essential Job Functions: •Serving as local business process owner (BPO) for several AZ quality system elements (e.g. change control, investigations, complaints, self-inspection, supplier quality management, etc.) to ensure their compliant and timely execution and continuous improvement. •Ensuring site operations, equipment, processes and product comply with local, regional, and corporate proc...more

From AstraZeneca Pharmaceuticals - 4/20/2018 5:50:18 AM

Manager, IT App Dev Commercial Application Systems

Amicus Therapeutics - Cranbury, NJ

Requirements • Bachelor's degree in computer science, computer information systems, or a related field (Equivalent education and work experience may be substituted.) • PMP/PMI or equivalent certification preferred. • 5+ years of experience leading projects that implement, develop and manage computer systems in regulated and non-regulated environments • Experience implementing and supporting a...more

From Amicus Therapeutics - 4/19/2018 12:59:21 PM

Manager, Quality Systems Administration and CSV Compliance

Amicus Therapeutics - Cranbury, NJ

Requirements - Bachelor's Degree in technical discipline or related field with minimum of ten (10) years' related experience. - Must have previous experience and proven track record of validating EDMS, Learning Management and QEM solution, preferably Master Control. - Strong understanding of the current pharmaceutical industry and applicable regulations, with emphasis in 21 CFR Part 11, 2...more

From Amicus Therapeutics - 4/19/2018 12:59:21 PM

Microbiology Manager

Amicus Therapeutics - Cranbury, NJ

Requirements - Bachelor's degree or advanced degree in Microbiology or related discipline. - A minimum of 10-15 years' experience working in a GMP QC Microbiology Laboratory, including significant clean room experience preferably in an aseptic processing facility. At least 2 years of management experience required. - Knowledgeable and/or exposure to biological manufacturing processes incl...more

From Amicus Therapeutics - 4/19/2018 12:59:21 PM

Quality Systems Associate I

Catalent Pharma Solutions - Kansas City, MO

The Role •Client Service; Answering window, phone or email, completing client (internal) requests in a timely manner.  Includes but is not limited to checking out documents or laboratory notebooks, providing electronic scans of whole or partial documents upon request and checking in documents or laboratory notebooks when delivered to the Records Center. •Electronic Data Entry; Entry of doc...more

From Catalent Pharma Solutions - 4/19/2018 5:45:03 AM

Food Project Microbiologist - Client Process Validation

Covance, Inc. a division of LabCorp® - Livermore, CA

Education/Qualifications B.S. or M.S. in Food Microbiology, Food Engineering or closely related area Experience 2-3 years of related experience in food industry or research and the ability to travel

From Covance, Inc. a division of LabCorp® - 4/19/2018 5:44:31 AM

Packaging Mechanical Technician - Trainee (2nd & 3rd Shift)

Merck & Co. - West Point, PA

Education: • Associate's Degree or higher in Applied Science - OR - High School Degree/GED in conjunction with equivalent Associate's Degree program or vocational certificate - OR -equivalent military course work NOTE: Equivalent programs will require training in courses such as: • Mechanical Pumps, Belts and Chain Drives • Lubrication and Installation of Bearings • Industrial Electr...more

From Merck & Co. - 4/19/2018 5:44:22 AM

Senior Specialist, Quality Assurance, Computer System Validation

Merck & Co. - West Point, PA

Education Minimum Requirement: • B.S. and/or M.S. degree in an appropriate Life Science, Computer Science, Information Technology or Engineering discipline. Required Experience and Skills: • Experience working in a Pharmaceutical/Biotechnology industry; experience working in a health authority regulated (e.g. GxP) environment. • A minimum of 5 years of industry experience including c...more

From Merck & Co. - 4/19/2018 5:44:22 AM

Engineer II QA R&D

Novartis Pharmaceuticals - Lake Forest, CA

Minimum Qualifications: •Bachelor's Degree or equivalent years of directly related experience •The ability to fluently read, write, understand and communicate in English •2 Years of Relevant Experience Our generous benefits package includes the Novartis Investment Savings 401(k) Plan which provides a company contribution of up to 6%. In addition, after one year of service, employees are eligible ...more

From Novartis Pharmaceuticals - 4/19/2018 5:43:43 AM

Process Validation Specialist

Catalent Pharma Solutions - Brussels, Région de Bruxelles-Capitale

The Role •Ensure that all qualifications and validations are performed according to the regulatory and customer requirements •Validation of aseptic process  (formulation, filling, holding times)  •Ensure that all activities are performed according to the schedule •Ensure that all activities are properly documented •Write qualification and validation protocols and reports and other do...more

From Catalent Pharma Solutions - 4/18/2018 5:48:52 AM

Equipment Technician

Catalent Pharma Solutions - San Diego, CA

The Role (daily responsibilities ) •Equipment Cleaning •Support disassembly of manufacturing equipment prior to cleaning •Participate in manufacturing equipment cleaning •Sample manufacturing equipment for cleaning verification •Prep solutions for manufacturing equipment cleaning •Document cleaning verification results and submit results for approval •Data entry and analysis •Calibrati...more

From Catalent Pharma Solutions - 4/18/2018 5:48:51 AM

Senior Quality Device Engineer

AstraZeneca Pharmaceuticals - West Chester, OH

Essential Job Functions: •Lead medical device and combination product Quality System initiatives at West Chester. Develop strategies, priorities, and plans as required. •Support activities related to the Combination Product and Medical Device Quality Management System, ensuring compliance to all applicable regulations. •Authoring, compilation and maintenance of Design History File content, C...more

From AstraZeneca Pharmaceuticals - 4/18/2018 5:47:39 AM
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