QC Lab Instrument Validation Engineer - San Diego, CA Job at Compli
QC Lab Instrument Validation Engineer - San Diego Area
(Pharmaceutical/Biotech)-Competitive Salary, Work/Life Balance!
On-Site / Pay W-2
Previous Pharmaceutical/Biotech/Medical Device experience is mandatory for these roles.
Are you looking to be a part of a close-knit work community? Do you have experience in the Life Science industry? Will you represent Compli, LLC as an experienced Validation Engineer for our pharmaceutical manufacturing, biotech, and medical device client projects? Do you enjoy traveling the country and making a difference? If so, this could be the right opportunity for you!
QC Lab Instrument Validation Engineer This position supports our client whose seeking an associate to support team members with 6 or more years' experience with validating lab instruments plus software.
Important: Our Client has mandated COVID-19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services to Compli' s client are required to comply with this requirement.
Important: Our Client has mandated COVID-19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services to Compli' s client are required to comply with this requirement.
Job Duties/Responsibilities:
6 or more years' experience with validating Lab Instruments and their associated software. Instruments include (HPLC’s (Agilent)c, FTIR’s, GC’s, UV Spectrophotometers, TOC Analyzers, Balances, etc.) Also, any validation with these type instruments involving data integrity and Part 11 compliance determination is a big plus.
Skills
A positive attitude and willingness to learn new concepts and new work knowledge required. Strong coordination and organization skill. Ability to write clearly and effectively. Strong verbal communication skills. Previous hands-on experience in equipment qualification is a plus. Working knowledge of Microsoft office as well as software used in analytical and bioanalytical instruments. Good organizational skills and detail oriented. Capable of completing assigned responsibilities within deadlines and keeping manager informed of status. Familiarity with GMP requirements and compliance, particularly good documentation practices.
Education
B.A. or B.S. degree (preferably in relevant scientific discipline) or an equivalent combination of education and experience.
Skills
A positive attitude and willingness to learn new concepts and new work knowledge required. Strong coordination and organization skill. Ability to write clearly and effectively. Strong verbal communication skills. Previous hands-on experience in equipment qualification is a plus. Working knowledge of Microsoft office as well as software used in analytical and bioanalytical instruments. Good organizational skills and detail oriented. Capable of completing assigned responsibilities within deadlines and keeping manager informed of status. Familiarity with GMP requirements and compliance, particularly good documentation practices.
Education
B.A. or B.S. degree (preferably in relevant scientific discipline) or an equivalent combination of education and experience.
Compli, LLC was founded in 2001 to provide commissioning, validation, and regulatory support services, CQV, asset management, reliability engineering, and staff augmentation services to the life sciences industry. We serve pharmaceutical companies across the U.S. Regarding regulations and compliance, it has never been more important to understand the documentation and quality assurance activities as they relate to vendors, engineering, construction, and contractors, which is why clients trust the Compli team.
Perks of the Job:
- Competitive Pay commensurate with experience
- Work / Life Balance
- Working with a small, close-knit team where you are valued as an individual
- A learning environment and continuous advancement opportunities
Feel overqualified? Feel underqualified? Apply anyway if this sounds like the fit you are looking for! We have flexibility in how we hire the role.
To learn more and APPLY NOW:
http://www.ucompli.com/careers
Agencies, Compli welcomes your qualified candidates. Please email
compli-opportunities@ucompli.com
to establish a relationship with our firm.
We are an equal opportunity employer M/F/D/V
Job Keywords: United States, San Diego, CA, CA, Surrounding Area, California, Validation Engineer, Technical Writing, CQV, Spectrophotometers, TOC Analyzers, Part 11 Compliance determination.
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