Reports To
GENERAL MANAGER CTC Budget
6 LPA Position Type
PERMANENT, ROTATIONAL SHIFT, PREFERENCE - MALE CANDIDATE Location
MANJUSAR, VADODARA, GUJARAT

Job Overview

1. Upstream and Downstream Fermentation Production Process
2. Monthly Production Batches Planning
3. To achieve Production Targets
4. Work Allocation to subordinates
5. Stock Coordination
6. Documentation
7. Inter Department Co-ordination

Responsibilities and Duties

1. Operation of both Upstream and Downstream process as per the batch plan
2. In-Process sampling and coordination with respective laboratories for results.
3. Assisting shift incharge for Production activities in Shifts
4. Perform assigned work on daily basis and report in clear manner
5. Maintain RM & consumables stock in coordination with Stores to avoid any Production delays
6. Arrange requisite resources for planned tasks and targets for the day
7. Supervising proper housekeeping of Production area

Soft Skills

• Leadership Quality
• Eye for detailing

Specific Skills

• Hends on experience in Fermentation
• Good Biotechnology knowledge

Experience 0-6 Years Education Qualification M.Sc. Biotechnology
B.E. Biotechnology
B.Tech. Biotechnology Preferred companies Biotech/Pharma Position Approved By Human Resource

Reports To
GENERAL MANAGER CTC Budget
1-4 LPA Position Type
PERMANENT, ROTATIONAL SHIFT, PREFERENCE - MALE CANDIDATE Location
MANJUSAR, VADODARA, GUJARAT

Job Overview

• Inoculum Preparation
• Inoculation
• In process sampling
• Periodic monitoring of swabs, samples, plates.
• Culture Maintenance

Responsibilities and Duties

• Responsible for aseptic inoculum preparation, transfer, sampling and sterility. Timely release of fermentation inoculum.
• Perform Periodic monitoring of facility (Settle plate, Swabs, Samplings, etc).
• Timely analysis, reporting to the Shift In charge during Production.
• Logical expression of plates, reporting and support to Production.
• Ensure that Culture is properly handled and maintained prior and post usage.
• Maintain all lab equipment in working condition and calibrated as per frequency.
• Maintaining proper housekeeping of the Production laboratory. Maintain it clean and contamination free.
• Ensure that Plant entry Log is maintained.
• Keep all records related to regulatory compliance updated.
• Training of technicians and workers to perform given tasks.

Soft Skills

• Leadership Quality
• Eye for detailing

Specific Skills

• Good microbiology knowledge and hands on experience.
• Knowledge of Good Documentation Practices.

Experience 1-4 Years Education Qualification M.Sc. Microbiology
M.Sc. Biotechnology Preferred companies Biotech/Pharma Position Approved By Human Resouce

Reports To
DEPUTY MANAGER CTC Budget
6-7 LPA Position Type
PERMANENT Location
MANJUSAR, VADODARA, GUJARAT

Job Overview

• Routine Microbial Analysis of Raw Material & Finish Good Samples
• Routine Calibration
• Environment Monitoring
• Media preparation
• Product Stability
• Documentation
• Report Preparation

Responsibilities and Duties

• Work planning and distribution to team members in a clear form.
• Prepare monthly, quarterly and annual sampling plan, Validation plan and/or qualification plan.
• Prepare and implement stability plan for all products.
• Management of resources on daily basis.
• Ensure proper upkeep and maintenance of instruments and facilities.
• Ensure Good Laboratory Practices are followed in the lab.
• Daily Reporting and release of Raw materials and finished goods.
• Co-ordination with warehouse for timely dispatch of pre-shipment and final shipment.
• Co-ordination with production to ensure batch schedule is executed in a timely manner.
• Ensure that periodic calibration and qualification of key equipment and instruments is completed.
• Co-ordination with QA for timely implementation of QMS and periodic Audits internal as well as extern

Soft Skills

• Leadership Quality
• Eye for Detailing

Specific Skills

• Good Microbiology knowledge and Hands on Experience
• Knowledge of Good Documentation Practices

Experience 6- 8 YEARS Education Qualification M.Sc. Microbiology
Preferred companies Biotech Or Pharma Position Approved By HR

Reports To
ASST. MANAGER - QA CTC Budget
up to 4.5 LPA Position Type
PERMANENT Location
MANJUSAR, VADODARA, GUJARAT

Job Overview

1. Documentation
2. BMR Review
3. Co-ordinate in validation activities
4. SOP Preparation, review and approval
5. Material approval as per Regulatory Guideline
6. Vendor Evaluation

Responsibilities and Duties

1. To exercise document and data control in the departments.
2. Review of BPRs, analytical document, in-process data, and Batch release.
3. Investigate customer complaint and Non-conformance issues.
4. Co-ordinate and execute all calibration and validation activities associated with QA, QC, Production etc.
5. Maintain documentation as per GMP, preparation, review and approval of SOP’s and related documents.
6. Handling QMS Documents, i,e Change control, Deviation,CAPA, Market complaint,Investigation of failures etc.
7. Vendor evealuation, review of BMR's, ECR's, euaipment qualifiation, Validation protocols and reports.
8. Shop floor exposure and knowledge of fermantation process.
9. Knowledge and experience of  regulatory/ certification audit i,e ISO, FAMI-QS, FSSC, Koshar, Halal etc.

Soft Skills

• Communication
• Problem solving
• Ability to multitask
• Attention to details
• Excellent follow up & coordination skills

Experience Minimum 5 Years Education Qualification M.Sc. Microbiology / Biotechnology Preferred companies Pharma / Biotech Position Approved By HR

Reports To
HEAD PRODUCTION Location
BHIWANDI

Job Overview Work in area of Biopesticide production Responsibilities and Duties

Planning and execution of activities during running of solid state fermentation (SSF) batches for different fungal strains. Timely delivery of production target and achieving the target and product quality Monitoring of Powder processing steps (harvesting, drying, fungal spore extraction, sifting & blending) critically to avoid any market complaints. Issuance of documents (BMR, Checklists, Equipment list, History card, Calibration records, etc.) Ensure all documents of plant are online. BMR, Checklists, Equipment list, History card, Calibration records, etc.) Maintaining batch wise data of SSF in soft copy form and submitting hard copies to higher authority whenever required. Raw material planning as per batch plan and requisition in time. Assisting Dept. Head in Training to the staff and helping training to workers. Ensure proper housekeeping of the entire Production area. Ensure Zero batch failure. To ensure effective implementation of the Safety Management System. To ensure continual improvement is facilitated using quality tool, Quality Management System, Total Productive Management, Safety policy.

Soft Skills Good communication & leadership skills. Specific Skills

ü  Manpower planning and controlling

Excellent knowledge and experience in biofertilizers, biopesticides product development. Experience 8-12yrs Education Qualification < Necessary education background > MSc  in Microbiology/Biotechnology/Agricultural/Life Sciences

Location
VADODARA

Job Overview We are seeking a Formulation Executive to support the development and scale-up of Neutraceutical formulation. The role involves hands-on formulation work in both oil- and powder-based dosage forms, along with responsibilities for encapsulation development. The candidate will play a key role in laboratory formulations then later into commercial production. Responsibilities and Duties

• Assist in the formulation development of Neutraceutical in oil suspensions, emulsions, and powder blends.
• Conduct trials for stability, solubility, and bioavailability optimization.
• Work with encapsulation to improve stability and delivery.
• Prepare technical documentation: batch manufacturing records, SOPs, formulation reports.
• Coordinate with technical expert, analytical teams, and production for scale-up and technology transfer.
• Support in selection of excipients, carriers, and packaging materials suitable for the formulations.
• Maintain compliance with Indian pharmacopeia, FSSAI, and international nutraceutical regulatory requirements.
• Ensure proper GMP practices are followed during formulation trials.

Specific Skills

• Strong formulation and analytical problem-solving ability.
• Practical lab/plant skills with an eye for precision and quality.
• Ability to work collaboratively with international consultants and internal teams.
• Excellent documentation and reporting skills.
• Adaptability to scale-up challenges in commercial manufacturing.

Experience 5-10 Education Qualification

• Master’s or PhD degree in Pharmaceutical Sciences
• 5–8 years of hands-on experience in nutraceuticals, dietary supplements, or pharma formulations.
• Strong exposure to oil- and powder-based formulations and encapsulation technology

Preferred companies Pharmaceutical, Nutraceutical