Molecular Diagnostic Manager
AI summary
Microhaem Scientifics is hiring a Molecular Diagnostic Manager in Kampala, Uganda. The role leads daily production of molecular diagnostic reagents, ensures GMP and ISO 13485 compliance, supervises production staff, and supports scale-up, validation, and quality testing. Candidates need a degree in Molecular Biology, Biotechnology, Biochemistry or a related field, at least 5 years of hands-on molecular diagnostic production experience in a GMP/ISO 13485 environment, and at least 3 years of leadership experience.
- Mid-level full-time role based in Kampala
- Leads molecular diagnostic reagent production and scale-up
- Requires GMP and ISO 13485 manufacturing experience
- Needs 5+ years hands-on experience and 3+ years leadership
- Degree in Molecular Biology, Biotechnology, Biochemistry or related field preferred
AI job guide
Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.
AI salary guide
Not enough public dataNot enough public salary data is available for this exact role. Before applying, prepare to ask about gross pay, benefits, contract length, probation period, transport and any allowances.
Can you qualify for this role?
- Required5+ 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 manager, full time, mid levelThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in Not specifiedThe 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 Molecular Diagnostic Manager evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Microhaem Scientifics and the role in Not specified.
- Add concrete examples related to manager, full time, mid level, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from BrighterMonday Uganda; avoid sending documents to unofficial contacts or copied links.
- Confirm the deadline, interview location and employer contact before sharing personal documents.
- Prepare a polite question about pay, benefits and contract terms for later interview stages.
Source and safety check
- BrighterMonday Uganda
- Original source link available
- Application method is clear
- Deadline not specified
- No major risk signal was detected in the captured text.
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Interview preparation
- What experience makes you a strong fit for this Molecular Diagnostic Manager role in manager, full time?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Not specified under the listed contract or schedule?
- Prepare examples with clear responsibilities, tools used and measurable outcomes.
- Review the source and research Microhaem Scientifics before the interview.
Ask what the first priorities will be in the role and how success will be measured.
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Original source description
- M
- Molecular Diagnostic Manager
- Microhaem Scientifics
- Quality Control & Assurance
- Yesterday
- New
- Kampala
- Full Time
- Manufacturing & Warehousing
- Confidential
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Experience
- Level:
- Mid level
- Length:
- 3 years
- Language Requirement:
- English
- Working Hours:
- Full Time - 8 to 5
- Applicant
- Location:
- Uganda
- Job descriptions &
- Bachelor’s or Master’s degree in Molecular Biology, Biotechnology, Biochemistry, or related field preferred.
- Minimum 5 years of hands-on
- in molecular diagnostic production in a GMP/ISO 13485-compliant manufacturing
- Minimum of 3 years’ leadership
- as a supervisor of molecular reagent production teams.
- Proven track record in scaling up molecular diagnostic reagent production, compliant with GMP/ISO 13485
- Minimum 5 years in molecular diagnostics manufacturing, with at least 4 years in GMP/ISO 13485-compliant manufacturing leadership
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Requirements
- DUTIES AND
- for open systems and/or closed molecular
- Document all production activities in compliance with ISO 13485 and/or WHO TGS/TSS
- Participate in method validation, verification, and technology development and transfer
- Identify opportunities for process optimization and cost reduction without compromising reagent
- Ensure SOPs and batch records are in place and consistently
- Oversee design and execution of performance evaluation studies (analytical and clinical).
- Champion contamination control strategies (cleanroom zoning, environmental monitoring).
- Work closely with R&D, QA, QC, and regulatory teams to support new product
- Train junior production staff on GMP/ISO 13485-compliant molecular reagent production techniques and GMP principles.
- QUALIFICATIONS &
Responsibilities
- Lead daily production of molecular diagnostic
- Ensure strict compliance with GMP, ISO 13485, SOPs, and quality
- Supervise and train production staff; plan manpower
- Oversee batch production records, documentation, and CAPA
- Monitor equipment performance, calibration, and preventive
- Drive workflow optimization and continuous process
- Lead scale-up of production from pilot to commercial batches, ensuring reproducibility and regulatory
- Implement electronic batch records and LIMS integration for
- Support incoming, in-process, and final QC testing