Job Description

States considered: Michigan

POSITION SUMMARY

The QO Laboratory Analyst supports routine testing and review of microbiology data in a GMP environment. The QO Lab Analyst works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze finished product samples prior to commercial release. This is a dynamic, growing lab within a growing manufacturing site with opportunity to learn new skills and to work cross-functionally.

POSITION RESPONSIBILITIES

• Analyzes raw materials, qualified utilities, APIs, and/or finished product samples in support of the company's quality program in the microbiology laboratory.
• Performs environmental monitoring.
• Supports microbiological programs including release/stability testing, sanitization/sterilization validation, media prep, and growth promotion.
• Performs, documents, record checks, and troubleshoots qualitative or quantitative assays on samples using techniques that vary from use of standard laboratory equipment to highly modern and automated instrumentation.
• Interprets and evaluates data in terms of accuracy, precision, trends, and potential GMP impact and recommends appropriate corrective action where necessary.
• Participates in laboratory investigations as required.
• This position may also be responsible for writing routine protocols or conducting assay, process, or instrument qualifications.
• The applicant may train others as skills and knowledge allow.
• Recommends and executes process improvements to continually improve laboratory performance.

TECHNICAL SKILLS REQUIREMENTS

• Must have demonstrated proficiency in aseptic technique.
• Ability to quickly learn new skills/techniques.
• High productivity and the ability to multi-task coupled with a low error rate and attention to detail are critical characteristics of this position.
• Must demonstrate flexibility/agility and engagement in a changing environment.
• The candidate is expected to display good laboratory technique to avoid cross-contamination or misidentification of samples.
• Able to comprehend and perform both routine and non-routine analyses from compendial and internal sources.

EDUCATION AND EXPERIENCE

• AAS or BA/BS in Microbiology, Biology, or related science preferred.
• Previous QA/QC experience in a GMP Pharmaceutical manufacturing environment desired.
• Preferred experience includes GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS
• Key characteristics of a successful candidate in this position: willingness and ability to learn, ability to work in a team environment, and attention to detail.

SHIFT HOURS

This position may require colleagues to work weekends and/or holidays to meet business or customer needs.

PHYSICAL REQUIREMENTS

Candidate must not be Cephalosporin/Penicillin sensitive.

While performing the duties of this job, the colleague is regularly exposed to both office settings and a laboratory setting. The work conditions for this position are 70% stationary and 30% standing and walking throughout the workday. The job duties involved occasional lifting (less than 35lbs).

Full time Regular Colleague

Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.

Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.

Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at [email protected] to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

Job Tags

Holiday work, Full time, Local area, Shift work, Weekend work,

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