Quality Assurance Officer
AI summary
Seeking a QA Officer to ensure cGMP compliance in a pharmaceutical manufacturing facility. Responsibilities include preparing SOPs, managing batch records, and handling deviations. Requires a science degree and 2+ years experience in the pharmaceutical industry.
- Mid-level position with 2 years experience required
- Salary range GHS 2,400 - 3,000
- Full-time, 8 to 5 working hours
- Location: Accra
AI job guide
Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.
AI salary guide
Source salary availableThe source lists GHS 2,400 - 3,000. Confirm the final pay, benefits, contract terms and allowances directly with the employer before accepting an offer.
Can you qualify for this role?
- Required2+ years of relevant experienceThe job post includes a minimum experience signal.
- RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
- PreferredPractical evidence in quality assurance, quality control, QA OfficerThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in AccraThe vacancy is associated with this location.
- UnclearComfort with the Full Time contract termsConfirm hours, duration, probation and benefits at the original source.
Documents to prepare
- Likely requiredUpdated CV
- Role specificCover letter or short employer message
- OptionalProfessional references
- Role specificAcademic or professional certificates
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Quality Assurance Officer evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Jobberman Ghana and the role in Accra.
- Add concrete examples related to quality assurance, quality control, QA Officer, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from Jobberman Ghana; avoid sending documents to unofficial contacts or copied links.
- Confirm the deadline, interview location and employer contact before sharing personal documents.
Source and safety check
- Jobberman Ghana
- Original source link available
- Application method is clear
- Deadline not specified
- No major risk signal was detected in the captured text.
Never pay for interviews, shortlisting, medical checks, uniforms, or job placement. Confirm every application at the original source before sharing personal documents. Report suspicious listing.
Interview preparation
- What experience makes you a strong fit for this Quality Assurance Officer role in quality assurance, quality control?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Accra under the listed contract or schedule?
- Prepare examples with clear responsibilities, tools used and measurable outcomes.
- Review the source and research Jobberman Ghana before the interview.
Ask what the first priorities will be in the role and how success will be measured.
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Use AI to apply better
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Original source description
Find a Job + + + + Search Quality Assurance Officer Eskay Therapeutics Limited Medical & Pharmaceutical 2 weeks ago Easy apply New Accra & Tema Region Full Time Manufacturing & Warehousing GHS 2,400 - 3,000 Negotiable Share link Share on WhatsApp Share on LinkedIn Share on Facebook Share on Twitter Share via SMS Job summary QA Officer will be responsible for ensuring cGMP compliance within the manufacturing facility Min Qualification: Degree
Experience
Location: Ghana Job descriptions &
Salary: GHS 2,400 - GHS 3,000
Location: Accra Log In and Apply Important safety tips Do not make any payment without confirming with the Jobberman Customer Support Team. If you think this advert is not genuine, please report it via the Report Job link below. Report Job Log in to apply now Continue with Google Continue with Linkedin Or continue with Forgot Password? Keep me logged in Log in Don't have an account? Sign Up to Apply Share link Share on WhatsApp Share on LinkedIn Share on Facebook Share on Twitter Share via SMS Activate Notifications Stay productive - get the latest updates on Jobs & News Activate Deactivate Notifications Stop receiving the latest updates on Jobs & News Deactivate This action will pause all job alerts. Are you sure? Cancel Proceed Similar jobs Lorem ipsum dolor sit amet consectetur adipiscing elit Lorem ipsum Lorem ipsum dolor (Location) Lorem ipsum Confidential 3 years ago Lorem ipsum dolor sit amet consectetur adipiscing elit Lorem ipsum Lorem ipsum dolor (Location) Lorem ipsum Confidential 3 years ago View More Stay Updated Join our newsletter and get the latest job listings and career insights delivered straight to your inbox. v2.homepage.newsletter_signup.choose_type Jobseeker Employer Email address * We care about the protection of your data. Read our Notify Me We care about the protection of your data. Read our privacy policy .
- Level: Mid level
- Length: 2 years Language Requirement: English Working Hours: Full Time - 8 to 5 Applicant
- with a pharmaceutical industry Working knowledge of cGMP is a must.
Requirements
Responsibilities
and Duties Preparation, development and review of Standard Operating Procedures. Assigning batch number, manufacturing and expiry date to drug products. Issuance of batch manufacturing record and batch packing record Preparation of master formula record, batch manufacturing record and batch packing record. Issuance and retrieval of monthly documents and format to respective department Review of preventive maintenance schedule Assessment, review and closer of change control and deviation Management of corrective and preventive action Preparation of annual product quality review Specimen signature management Incident handling Qualifications Science Graduate Minimum of 2 years' work