Senior Officer
AI summary
Sun Pharma is hiring a Senior Officer in the Production (Docs Cell) unit at its Toansa site in Uganda. The role focuses on change control, validation and qualification documentation, training coordination, and ensuring cGMP and SOP compliance. Candidates need an M.Sc. in Chemistry and 5–8 years of API plant experience.
- Senior-level role in pharmaceutical production documentation
- Focus on change control, validation and qualification activities
- Requires M.Sc. Chemistry and 5–8 years API plant experience
- Strong knowledge of cGMP and FDA regulations needed
- Full-time position based in Toansa, Uganda
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 Confidential. Confirm the final pay, benefits, contract terms and allowances directly with the employer before accepting an offer.
Can you qualify for this role?
- Required5+ years of relevant experienceThe job post includes a minimum experience signal.
- PreferredPractical evidence in cleaning, technology, IT, Software & DataThe 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
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Senior Officer evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Sun Pharma and the role in Not specified.
- Add concrete examples related to cleaning, technology, IT, Software & Data, 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.
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 Senior Officer role in cleaning, technology?
- 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 Sun Pharma 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
- S
- Senior Officer
- Sun Pharma
- IT, Software & Data
- Today
- New
- Full Time
- Manufacturing & Warehousing
- Confidential
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Experience
- Level:
- Senior level
- Length:
- 5 years
- Language Requirement:
- English
- Working Hours:
- Full Time - 8 to 5
- Applicant
- Location:
- Uganda
- Job descriptions &
- Tenure : 5 - 8 Years in API Plant, Strong knowledge of cGMP, FDA regulations, and industry best practices
- Your Success Matters to Us
- At Sun Pharma, your success and well-being are our top priorities! We provide robust
- and background of incumbent(s).
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Requirements
Job Title
Senior Officer
Business Unit
Production (Docs Cell)
Job Grade
G12B
Location :
Toansa
At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Key
Educational Qualification
M.Sc. (Chemistry)
Responsibilities
Initiation, review and QA approval of change controls related to process, equipment and facility in TrackWise system for all the modules/Dept. to fulfill the production requirement at Toansa site.
Preparation of draft MPRs/BRCs along with necessary data as per the production requirement of modules at Toansa site.
Uploading of draft MPRs/BRCs in BPR Printing Module for implementation and release.
Preparation, review and QA approval of validation/qualification protocols, reports, PPV, SPR, temperature mapping, product manuals, plant development reports, Cleaning matrix, CPDR, Equipment suitability, HAZOP, Investigations (OOS/OOT/UPD) as per current SOPs for all the production modules at Toansa site.
To coordinate with Production modules effectively for collection of supporting data / documents for CCR / Validation / Qualification related activities to complete the record as per the requirement.
Tracking the completion of the activities as per the actions items for closure of CCRs/Protocols as per the dues dates. Wherever applicable, provide suitable justification for extension of records in TrackWise.
To prioritize CCRs/Validation/Qualification related work to align with the production commitments.
To harmonize documentation practices related to CCRs, Validation & Qualification activities at site.
To ensure good quality documentation work as per GDP so as to minimize document review and approval time. Maintain very good productivity level in all assigned documentation related activities.
Escalate any delays/bottleneck in completing documentation work to the concerned operating manager and team leader.
Practicing company values in all aspects of work.
Ensuring compliance to cGMP, current SOPs and Safety procedures, as applicable, in the related areas.
Adherence to schedules to avoid any deviation and ensure for compliance.
Ensuring timely completion of assigned trainings in LMS.
Responsible for all training related to Document Cell.
To assign Training activities to Job Roles.
To review completion of Job Specific Trainings (as applicable).
Responsible for organizing training sessions in department, creating the sessions in LMS and punching the attendance in system.
Maintaining all record related to training.
Tracking pending trainings and ensuring training completion through continuous follow-up.
Travel Estimate
Job
Benefits
and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!
Disclaimer:
The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the