QC Lab Technician – Entry Level (GMP/GLP)

Collabera

Scarborough (ME)

In loco

GBP 21.000 - 26.000

Tempo pieno

10 ore fa
Candidati tra i primi

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Vantaggi offerti da questo lavoro

Medical insurance
Dental insurance
Vision insurance
401(k) retirement plan
Life insurance
Disability insurance
Paid parking/public transportation
Paid time off

Descrizione del lavoro

Collabera is seeking an entry-level QC analyst based in Scarborough, ME, onsite. You will join the Quality Control team, performing in-process and final testing of diagnostic products, and supporting documentation and calibration tasks.

Ideal candidates have a life sciences background, hands-on lab exposure, and a willingness to learn. Regulatory exposure is a plus, and MS Word/Excel skills are expected for documentation.

Competenze

  • Associate or Bachelor’s degree in Biology, Chemistry, Life Sciences, or related field or equivalent education/experience.
  • Hands-on laboratory exposure in academic, industrial, or technical environments.
  • Basic understanding of laboratory procedures, testing, and documentation.
  • Strong attention to detail, problem-solving abilities, and eagerness to learn.
  • Basic computer skills, including MS Word and Excel.

Mansioni

  • Perform in-process and final testing of Lateral Flow, ELISA, and Molecular products.
  • Operate laboratory equipment, conduct procedures, and troubleshoot issues as they arise.
  • Review batch records and maintain accurate testing documentation.
  • Calibrate and maintain laboratory equipment.
  • Follow GMP/GLP and safety procedures, maintaining quality standards.
  • Support QMS activities and continuous improvement initiatives.

Conoscenze

Attention to detail
Problem-solving
Willingness to learn
MS Word & Excel

Formazione

Associate or Bachelor’s in Biology, Chemistry, Life Sciences

Strumenti

Pipettes
pH meters
ELISA assays

Descrizione del lavoro

Collabera is seeking an entry-level QC analyst based in Scarborough, ME, onsite. You will join the Quality Control team, performing in-process and final testing of diagnostic products, and supporting documentation and calibration tasks.

Ideal candidates have a life sciences background, hands-on lab exposure, and a willingness to learn. Regulatory exposure is a plus, and MS Word/Excel skills are expected for documentation.

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