Role & responsibilities This role will be responsible for the maintenance of overall plant Electrical equipments, instrumentation & calibration and electrical installation in new projects. Key Deliverables: a) Day to day monitoring & maintaining record of electrical power consumption.b) Schedule and undertake preventive maintenance of all equipment and instruments.c) To attend electrical breakdowns and provide solution to breakdown and troubleshooting.d) Schedule and carry out calibration/ validation of instruments / equipments.e) Coordination with electrical consultant & vendors for electrical drawing, specifications for maintenance & project work. f) Assist in purchase of electrical components / spares. g) Assist in new projects, do electrical load calculation and prepare BOQ as per requirement.h) Supervise electrical activities of new projects.i) Repairs to residential flats at company guest houses is part of job. Non-electrical jobs may also be assigned. Functional Competencies:a) Hands on experience in electrical installations.b) Experience in HVAC, DG Sets, Chillers, Transformer, HT/ LT Panels etc.c) Experience of PLC, SCADA and its trouble shooting.d) Knowledge of ISO & GMP documentation and Audit compliance.e) Knowledge of SAP (Purchase Module).Behavioural Competencies:a) Quality and Service Orientation.b) Customer Centricity (Internal Customer).c) Cross-Functional Team Working.d) Good Communication.e) Drive for Consistent Results.Preferred candidate profile Degree or Diploma holder in Electrical or Industrial Electronics with 5+ years of experience in Pharma / Medical / Food sectors. Perks and benefits 1. Opportunity to work at Head Office location.2. Intimate small company culture. 3. Five days working (alternate weeks).4. Medical Insurance for spouse and children.5. Housing accommodation for Bachelors & family.

Role & responsibilities You shall be responsible for maintaining and improving all QMS activity, GMP and GLP across the company. Key Deliverables:1. Ensure manufacturing practices as per cGMP and GLP standards.2. Handling QMS activities like change control, validations, stability, qualifications, APQR and Risk assessment etc.3. Applications for AHC to AQCS, EIA and Capexil and coordinate related activities. (AHV/SPD: This is exclusive knowledge related to Capsule and companies manufacturing animal origin products. We have mentioned this as the candidate on joining will be responsible for this work though he/she may not be having exposure to same.)4. Organize internal and external audits for ISO, GMP+, FDA, Capexil, GMP+, EIA and others. Maintain the documents required for those audits.5. Ensure all personnel are trained on requirements for GMP, GLP, GDP, applicable regulatory issues and other procedures related to their work area. (SBG)6. Evaluation and approval of Suppliers for RM, PM, testing labs and service providers.7. Assisting HOD in customer complaint analysis and preparation of customer complaint report. 8. Investigation of incidents, deviations, OOS and ensure corrective actions in place. 9. Reviewing the daily availability of operators and allocating work to them.10. Maintaining and review BMR documents, guide for relevant changes if required.11. Label artwork review and management.Technical Competencies:a) Analytical skills (spotting trends and patterns)b) Report writing skillsc) Problem solving abilitiesd) GMP and GDP knowledgee) Good English communication skills (verbal & written).Behavioural Competencies:a) Quality and Service Orientationb) Delivering consistent resultsc) Ability to prioritize, organize, manage work and time. d) Customer Centrice) Cross Functional Team Working Preferred candidate profile B. Pharma, B.Sc./M.Sc. (Chemistry/Microbiology)8+ Years of experience in QA process in Pharmaceutical / food processing / cosmetics / chemical industries.Perks and benefits 1. Opportunity to be part of a growing organization offering niche products to Pharma industry.2. Opportunity to work at Head Office location.3. Intimate small company culture with MNC professionalism. 4. Company value programs TrANSSCEnD.5. Employee events like festival celebrations, family fun events etc.6. Five days working (alternate weeks).7. Medical Insurance for your immediate family.8. Housing accommodation for Bachelors & family.

Role & responsibilities A. Principal thrust area: a. To prepare Manuals, Instructions, and Video Scripts for CCPL products explaining how to use them. b. Coordinate for work with Factory Team in India & Sales Team in USA and outside photographer / videographer.B. Key Deliverables: a. Understand product functions to prepare or upgrade high quality operating Manuals, Instructions, & Videos (documentation) to align with world-class standards, enhancing clarity, readability, and user-friendliness for international customers.b. Validation of the documentation individually in front of the product from the users perspective.c. Verify documentation with technical and non-technical associates to check whether it is clear and easy to understand. Update them based on feedback. d. Ensure alignment of text with photos and use of consistent terminology. Use correct grammar and spelling. e. Coordinate and supervise Photography and Videography by professionals. Should be able to do basic photography and video shooting. Should be able to do basic photo and video editing or willing to learn same. f. Write scripts for videos and get videos made for new & existing products.g. Timely update the style guide and follow for consistency in documentation.h. Work in collaboration with documentation and marketing associates at our USA office.i. Explore the latest trends in documentation and collaborate with third-party experts.C. Competencies:C1. Technical Competencies:a. Competent in Technical Content writing. b. Good in planning & prioritizing work.c. Quick learner for understanding the equipment functions.d. Photo/Video capturing and editing experience required.e. Knowledge of end-user documentation / product documentation / technical documentation/Video Documentation. Experience in product documentation for overseas products is added advantage.C2. Behavioural Competencies:a. Attention to detail and a desire for perfection. c. Self-driven with expertise in product description skill.d. Logical thinking and organized thoughts.e. Cross Functional Team Working Skills.f. Quality and Service Orientation.g. Delivering Consistent Results.D. Reporting & Responsibility: Position Reports to: Manager Techno Commercial Manager (M05)Reportees to this Position: Officer Technical Writer (M11).E. Job Location:1. Tarapur MIDC. Tarapur MIDC, Boisar, Dist. Palghar, Maharashtra. a) Preference will be given to candidates in Tarapur/Boisar area or willing to relocate.b) Candidates (Mumbai/Western Suburbs on case to case basis) who can work on-site a minimum of 4 or more days/week will be considered. 2. For outstation bachelors, company provides a subsidized bachelors flat with a cook. For outstation families, company provides subsidized accommodation in company owned buildings. Relocation allowance is offered.3. Tarapur- Railway station Boisar takes 1.5 hrs. by train from Borivali Station or by road via Western Express Highway. 4. Suburban local trains direct from Churchgate to Boisar Railway station available.Preferred candidate profile You must be: 1. Diploma Mechanical or Graduate / Post Graduate in Science / Pharma (English medium with convent schooling preferred).2. Having 8+ years of product documentation experience. Preferably from Pharmaceutical / Medical device / FMCG / Food manufacturing industry.Perks and benefits 1. Opportunity to be part of a growing organization offering niche products to Global Pharma industry.2. Opportunity to work at Head Office location.3. Intimate small company culture with MNC professionalism. 4. Company value programs TrANSSCEnD.5. Employee events like festival celebrations, family fun events etc.6. Five days working (alternate weeks).7. Medical Insurance for your immediate family.8. Opportunity to work closely with US Director.