...programs for major capital projects.
Commission, qualify, and validate facilities, utilities, and/or equipment in assigned projects.... ...-7 years of applicable work experience in the biomedical and pharmaceuticals industry.
~ Proficient in authoring and executing DQ, FAT,...
Suggested
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For contractors
Work experience placement
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Local area
...your future.
Your Role
We are hiring an experienced Validation Engineer to support multiple commissioning, qualification, and... ...procedures, reports, risk assessments, and so on for a range of pharmaceutical and manufacturing equipment, facilities, utilities, and...
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Full time
For contractors
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Local area
...Job Description
Job Description Salary: TBD
Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology industries.
Our Computer Systems Validation Leads work directly with our clients to support activities that include...
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Full time
Contract work
...documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and execution... ..., purification, recovery, building automation or other pharmaceutical manufacturing processes
Other Requirements:
Excellent oral...
Suggested
Full time
Worldwide
Relocation
...biopharmaceutical manufacturing? If so, this Biologics Process Validation Leader role could be an ideal opportunity to explore.
As... ...Minimum 5 years' demonstrated experience in the Pharmaceutical Industry in leading the technical aspects of the product lifecycle...
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Local area
...Job Description
Job Description Salary: Hourly TBD
Quality Agents, LLC is a service company offering validation and quality expertise to the pharmaceutical and biotechnology industries. Our Validation Engineers will be involved with the qualification and...
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Hourly pay
Holiday work
Full time
...Job Description
Job Description This position supports site projects and ongoing validation. Primarily responsible for the design, authorship, and execution of commissioning, qualification and/or validation studies for any or more of the following major disciplines...
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For contractors
Immediate start
Visa sponsorship
...to perform this position if required by a specific state.
* Valid driver's license and acceptable driving record.
* Legally authorized... ...skills/preferences:
* Two or more years of sales experience (pharmaceutical or non-pharmaceutical) after completion of an undergraduate...
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Full time
Work experience placement
Local area
Flexible hours
...opportunity to implement cutting-edge technology into biological and pharmaceutical products and processes.
Skills & Requirements:
BSc in... ...and good working knowledge of method development, method validation/qualification.
Experience with GMP laboratory operations....
Suggested
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...opportunity to implement Client technology into biological and pharmaceutical products and processes.
Key responsibilities:... ...patients.
Design and execute method development and GMP validation for recombinant factor C endotoxin testing.
Contribute to...
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...great opportunity for those wanting to start their career in Pharmaceutical manufacturing getting exposure to both critical functions Manufacturing... ...discriminated against on the basis of disability. AbelZeta validates right to work using E-Verify. Salary at AbelZeta is...
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...with a strong background in selling professional services in validation, quality, engineering, and related. Seeking excellent communication... ...in an engineering or project management role within pharmaceutical manufacturing and biotechnology is strongly preferred.
Minimum...
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Flexible hours
...customized end-to-end chain of custody solutions for our large pharmaceutical clients and partners in academia and government, ensuring the... ...Requires 2+ years driving experience in a similar role.
Requires valid Commercial driver's license Class B (CDL B) and a good driving...
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...MacroGenics facilities.
Supports execution of new equipment validation tests and modification and validation of existing equipment... ...related manufacturing and/or laboratory equipment in a biotech or pharmaceutical company.
Prior experience with the troubleshooting and...
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For contractors
Relocation
...molecules, as well as late stage process characterization and validation. As a key member of our leadership team, this role will... ...Experience
~ PhD in Biochemistry, Chemistry, Chemical Engineering, Pharmaceutical Sciences, life sciences or equivalent amount of experience...
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...written procedures and limited non-routine testing including validation studies with supervisory oversight.
Perform environmental... ...Microbiology/Biology or related field
Experience: 2-4 years in the Pharmaceutical or Biotechnology with emphasis in aseptic processing, QC...
...Participate in activities as defined in method transfer/qualification/validation/stability study protocols.
Review, analyze, interpret, and... ...in a Quality Control work environment, preferably in the pharmaceutical industry with knowledge of cGMP is a plus
Considerable...
Contract work
Work experience placement
...Operating Procedures (SOPs) and User Guides.
Review documents, validate trial information, abstract relevant protocol or scientific... ...Degree
A minimum of two (2) years experience in a pharmaceutical, biotechnology and/or clinical environment which includes medical...
Casual work
Local area
Remote job
Work from home
Flexible hours
...is responsible for development, evaluation, qualification and validation of methods and testing of reference materials to support... ...characterization are preferred.
•Working experience in the pharmaceutical, biotechnology or life sciences industry is preferred.
•Working...
For contractors
Work experience placement
Worldwide
...Design, support, and lead QC testing related to Aseptic Process Validation (APV) and Aseptic Operator Validation (AOQ).
Design and... ...work environment, preferably in a regulated environment in the pharmaceutical/biotech industry.
Working knowledge of cGMP regulations....
Holiday work
Contract work
Temporary work
...~ Bachelor of Science in Biochemistry, Chemistry, Biology, Pharmaceutics Engineering or related scientific filed
~5+ years industrial... ...proteins
~ Experience with GMP's, ICH Guidelines and FDA/EU validation practices for biopharmaceutical processes
~ Experienced in...
Local area
...airport, and be able to travel overnight 60-80% as business requires.
Must have a current and valid driver's license.
Demonstrates an understanding of pharmaceutical industry practices, as well as standard medical practices in therapeutic area(s) of concentration...
Local area
Work from home
Home office
Night shift
...global projects as team portfolio evolves. Fluency in (bio)pharmaceutical processes, facilities, operations, market developments, engineering... .... Knowledge of cGMP and market trends in automation, validation, construction to ensure project execution excellence and continuous...
Contract work
For contractors
Local area
...Job Description
Job Description Salary: TBD DOE
Quality Agents, LLC is a service company that offers validation and quality expertise to the pharmaceutical and biotechnology industries. We accept applications on an on-going basis in order to build a talent pool...
Holiday work
Full time
Otsuka Pharmaceutical Company is a global healthcare company with the corporate philosophy: "Otsuka-people creating new products for better... ...employee directly or through Otsuka's application portal without a valid written search agreement in place for the position will be...
Contract work
Local area
Remote job
Worldwide
Flexible hours
...appearance)
• Contribute to generating SOP’s and qualification/validation/transfer protocols and reports
• Responsible for cross... ...group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination...
Hourly pay
Contract work
Worldwide
Work alone
Flexible hours
...processes related to cGMP such as Commissioning, Qualification and Validation (CQV), Computer System Configuration Management and Computer... ...or Drug Product).
Knowledge of quality systems and pharmaceutical regulatory requirements (21 CRF Part 11/210/211, ICH 8, ICH 9...
Holiday work
Contract work
Temporary work
Shift work
...materials, in-process materials and finished products. Method validations and transfers, laboratory animal facility management,... ...10 years’ experience in Management in Vaccine, Biologics or Pharmaceutical testing facility.
Knowledgeable of FDA/ICH/EU regulations...
Contract work
Local area
...Manufacturing Technician
Main Points
~1 year experience in medical device field or pharmaceutical field
~ Need to have 1 year experience in manufacturing environment
~ Knowledge of GMP
~ Knowledge of Six Sigma and ISO
Job Description
You will be responsible...
...materials.
Requirements:
High School Diploma or equivalent with exposure to science and math coursework and a minimum of three years of related experience in the biotech/pharmaceutical industry
Prior experience following GMP rules and procedures a plus...
Contract work
Immediate start