Senior Manager Production
About this opportunity
Job Description
Followings will be the Coe Job responsibilities of the position holder:
Compliance to laid standards of current Good Manufacturing Practices (cGMP).
Carrying, review and approval of qualification of production equipment.
Ensure compliance with specifications and validated methods.
Training and evaluation of the Management and Non-Management staff for the qualification to specific task or to operate specific equipment.
Preparation and review SOPs for related equipment’s and procedures.
Raising, review of requisition for the requirement of consumables items and check on its inventories according to their approved budget.
Implementation of Quality Management Systems as per cGMP and international standards.
Implementation of Corrective and Preventive Actions (CAPA) for non-conformances and self-inspection findings.
To exercise effective control over environmental conditions in manufacturing and other related activities, which may adversely affect the product quality.
To Coordinate and approve calibration/maintenance of all production equipment’s and instruments with engineering / QA / QC and outside agencies.
To carry out routine documentation per regulatory requirements.
Adhere to specified working hours.
To ensure and maintain cleanliness of production areas and equipment as per SOPs.
Coordinate with production, PPIC, QC, CQA, PLM, QA and others for smooth production activities.
Organize the job responsibilities to the technicians, officers, executives, assistant managers as per plan and to manage absenteeism.
Verification of dispensed input materials against process orders.
Continuous monitoring of in-process controls in all production areas. Continuous monitoring and improving production output on daily basis.
To fill, maintain and approve BPR/BMR online and to ensure online SAP entries.
To evaluate and sign production records before QA submission.
To review production and related documentation.
To Monitor and control of manpower utilization, yield, waste, and Opex.
To Ensure audit readiness and regulatory compliance.
Handling of online systems and software and ensure review and approval in systems like SolTRAQs, ISOtrain, Darius, Brainshark, Harmony etc.
Ensure the compliance of SAP activities related to updation of BOM, creation of new item codes, batch transactions etc.
Ensure compliance with BBS and BBQ.
To conduct self-inspection/internal audits as per site Internal Audit Program. To Investigate and provide CAPA for audit observations (internal and external). To conduct cGMP and GDP training in LVP facility.
In absence of the position holder, the sub-ordinate / assistant Manager working in the section, or the authorized designee (as applicable) shall be responsible for day to day working.
Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 514 comparable Manager Manufacturing & CMC roles across 76 biopharma companies.
Salary context
156 of 514 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 514 comparable roles
+ 32 more countries
Seniority mix
514 of 514 peers have a known seniority level
Therapeutic area mix
6 of 514 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.