Quality Control Document Reviewer Level 2 at SGS

Markham, Ontario, Canada -

Full Time

Start Date

Immediate

Expiry Date

16 Feb, 26

Salary

0.0

Posted On

18 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Control, Documentation Review, Analytical Methods, SOP Compliance, LIMS, Pharmaceutical Testing, Communication Skills, Attention to Detail, Problem Solving, Data Review, Validation, Method Transfer, OOS Management, Team Collaboration, Time Management, Technical Writing

Industry

Professional Services

Description

Company Description We are SGS – the world’s leading testing, inspection, and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer, and more interconnected world. Job Description Assures that reviewed Quality Control records are compliant to methods, specifications and company’s applicable Standard Operating Procedures. The review is done according to QAM-210 Data Review SOP Identifies area for improvement of SGS SOPs, analytical methods and forms. Follows deadlines specified on a lab sheet or as scheduled by their supervisor. Assures records of Validation/Method Transfer/Verification and reports are as per protocol and method provided by clients or written by SGS Assures that OOS and deviation are closed before forwarding the records to QA for release of C of A. Issues an audit form noting deficiencies to method and procedures, returns the form to analyst for correction according to Data Review SOP; Ensures that all valid deficiencies are corrected; escalates all concerns to management. Ensures that documentation review is complete in every respect and reviews that all results are entered into the electronic laboratory information system LIMS. Qualifications Education: Bachelor of Science degree (or equivalent combination of education and experience such as College with 10 years of pharmaceutical QC testing/records review experience) in Chemistry, Biochemistry, Biology, Microbiology or related biological science or equivalent in job experience Experience: over 2 years’ experience working in a pharmaceutical regulated Laboratory environment or Pharmaceutical company. Comfortable with electronic systems (eg. LIMS) and other lab equipment to be able to perform audit trail of testing records Shift work may be required Ability to learn quickly in a challenging environment. Excellent language, writing and communication skills required. Additional Information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression and Indigenous status, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities, or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. Accommodations are available on request for qualified candidates during each stage of the recruitment process. Please note that candidates applying for Canadian job openings should be authorized to work in Canada.

Responsibilities

The role involves reviewing Quality Control records to ensure compliance with methods, specifications, and Standard Operating Procedures. The reviewer identifies areas for improvement and ensures all documentation is complete before forwarding records for QA release.