2910 Clinical Laboratory jobs in Alameda,CA

Competitive remuneration, annual incentive plan bonus

The salary range estimated for this position based in California is $93,000.00–$98,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy.

Healthcare

A choice of national medical and dental plans, and a national vision plan, including health incentive programs

Employee assistance and family support programs, including commuter benefits and tuition reimbursement

At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

Standard (Mon-Fri)

Must be legally authorized to work in the United States without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, Chemical Engineering, or similar In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years')

Minimum 5 years of experience in biologics, biotechnology, pharmaceutical manufacturing, quality control, quality systems, supplier quality, or raw materials management.

Demonstrated experience authoring specifications within a GMP-regulated environment.

Experience reviewing Certificates of Analysis, supplier quality documentation, and technical data packages.

Strong understanding of GMP regulations and ICH guidelines

Experience with electronic quality systems, document management systems, ERP systems, and/or LIMS.

Able to work upright and stationary and/or standing for typical working hours.

Able to lift and move objects up to 25 pounds

Able to work in non-traditional work environments.

Able to use and learn standard office equipment and technology with proficiency.

The successful candidate will preferably have strong experience in GMP documentation, and biologics raw materials.

Experience supporting startup, expansion, or commissioning of a QC laboratory.

Experience with equipment qualification

Knowledge of USP, EP, JP, and other compendial requirements related to raw materials.

Experience with supplier qualification, supplier audits, and change management programs.