Lead QA Technician

at  Thermo Fisher Scientific

Rockville, MD 20850, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate18 Dec, 2024Not Specified23 Sep, 20242 year(s) or abovePharmaceutical IndustryNoNo
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Description:

JOB DESCRIPTION

Conducts critical reviews of GMP documentation associated with materials control (material specifications, receipt inspection forms, inventory records) by exercising judgment within defined procedures and regulations.
 Assure all activities are in accordance with the batch records, departmental SOPs, GMP and DEA regulations.
 Review of online batch records in terms of completeness of signatures, entries, and material reconciliation.
 Approves and controls labels.
 Reviews documents completed by operations personnel
 Resolves production/QC and documentation discrepancies.
 Responds to inquiries on quality control activities and schedules in general.
 Collects and trends Quality Control Data and maintains the QC Shipping & Receiving Logs.
 Host internal and external audits, provide timely CAPA plans in response to any audit observations, and track CAPAs to completion.
 Other duties may be assigned to meet business needs.

Education/Experience:

  • Requires a bachelor’s degree in a life sciences discipline
  • Prefer 5+ years’ experience within biological, biopharmaceutical, or regulated pharmaceutical industry
  • 2+ years’ experience in QA/QC function
  • Requires thorough knowledge of cGMPs, 21 CFR, Part 210/211/600s, USP and ICH guidelines.

At Thermo Fisher Scientific, we are committed to creating a workplace where diversity and inclusion are valued. We believe that bringing together individuals with different experiences, backgrounds, and perspectives leads to innovative solutions and better outcomes for our customers. As an equal opportunity employer, we strictly prohibit discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.
We also offer accessibility services for job seekers requiring accommodations in the application process. If you require assistance due to a disability, please contact us at 1-855-471-2255* to request an accommodation.

Responsibilities:

Please refer the Job description for details


REQUIREMENT SUMMARY

Min:2.0Max:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

A life sciences discipline

Proficient

1

Rockville, MD 20850, USA