Author: Sudheer vanguri

Vimta Labs Walk-In Drive for Freshers – 35 Vacancies

Vimta Labs is conducting a Walk-In Drive for Freshers for opportunities in its laboratory and contract research operations in Hyderabad, Telangana. The recruitment drive offers 35 positions for candidates with B.Pharmacy or M.Sc. Chemistry qualifications. Eligible candidates can attend the walk-in interview on 27 September 2026 at the Vimta Labs Limited campus. Candidates with active backlogs are not eligible for this recruitment drive.

Walk-In Interview Details

Company

Vimta Labs Limited

Recruitment

Walk-In Drive for Freshers

Vacancies

35 Positions

Experience

Freshers

Interview Date

27 September 2026, Sunday

Interview Time

9:30 AM to 12:00 PM

Work Location

Shameerpet & Cherlapally, Hyderabad

Candidates may be deployed to other locations based on business requirements.

Eligibility & Qualifications

Educational Qualification

Candidates with the following qualifications are eligible:

• B.Pharmacy
• M.Sc. Chemistry – Analytical, Organic, or Inorganic
• 2025 & 2026 passed-out candidates

Eligible Qualification Courses

B.Pharm | M.Sc. Chemistry | M.Sc. Analytical Chemistry | M.Sc. Organic Chemistry | M.Sc. Inorganic Chemistry

Walk-In Recruitment Process

The recruitment drive is intended for freshers looking to begin their careers in the contract research and testing industry.

Selected candidates may work across Vimta Labs’ operations at Shameerpet and Cherlapally, Hyderabad, with deployment to other locations depending on business requirements.

Important Instructions

Candidates attending the walk-in interview should follow these instructions:

• Carry an updated resume.
• Work timings will be based on shift requirements.
• Formal dress code is required.
• Candidates with active backlogs are not eligible.

Walk-In Venue

Vimta Labs Limited
142, Cherlapally Main Road,
IDA Phase II, Cherlapally,
Hyderabad, Secunderabad,
Telangana – 500051

How to Apply

Interested and eligible freshers can attend the Vimta Labs Walk-In Drive directly at the above-mentioned venue on 27 September 2026, between 9:30 AM and 12:00 PM.

Candidates should carry their updated resume and attend in formal attire.

Job Summary

Symbiotec is conducting a Walk-In Drive in Vadodara for multiple openings across Production/R&D, Quality Control, and Quality Assurance functions.
The recruitment covers Upstream, Downstream, QC (IPQC/HPLC/Wetlab/GC), and QA positions with experience requirements from 1 to 12 years.
Candidates with M.Tech, M.Sc., B.Tech., B.Pharm., and M.Pharm. qualifications can apply for the relevant positions.
The walk-in interview is scheduled for 20 September 2026, from 9:00 AM to 4:00 PM, with applications closing the same day.

Symbiotec – Upstream Production / R&D Department

Jr. Executive – Upstream

Vacancies: 07
Location: Ujjain / Indore
Qualification: M.Tech. / M.Sc. / B.Tech. in Biotechnology / Microbiology / Biochemistry
Experience: 1–3 Years

Symbiotec – Upstream Areas of Work

• Classical fermentation
• Fermentation-derived APIs
• Batch fermentation
• Fed-batch fermentation
• Scale-up
• Fermentation monitoring

Symbiotec – Upstream Production / R&D Department

Executive – Upstream

Vacancies: 07
Location: Ujjain / Indore
Qualification: M.Tech. / M.Sc. / B.Tech. in Biotechnology / Microbiology / Biochemistry
Experience: 3–6 Years

Symbiotec – Upstream Production / R&D Department

Sr. Executive – Upstream

Vacancies: 07
Location: Ujjain / Indore
Qualification: M.Tech. / M.Sc. / B.Tech. in Biotechnology / Microbiology / Biochemistry
Experience: 6–10 Years

Symbiotec – Upstream Production / R&D Department

Assistant Manager – Upstream

Vacancies: 07
Location: Ujjain / Indore
Qualification: M.Tech. / M.Sc. / B.Tech. in Biotechnology / Microbiology / Biochemistry
Experience: 10–12 Years

Symbiotec – Downstream Production / R&D Department

Jr. Executive – Downstream

Vacancies: 07
Location: Ujjain / Indore
Qualification: M.Tech. / M.Sc. / B.Tech. in Biotechnology / Microbiology / Biochemistry
Experience: 1–3 Years

Symbiotec – Downstream Areas of Work

• Purification
• Column chromatography
• Continuous centrifugation
• High-pressure chromatography
• Low-pressure chromatography
• Tangential Flow Filtration (TFF)
• Lyophilization

Symbiotec – Downstream Production / R&D Department

Executive – Downstream

Vacancies: 07
Location: Ujjain / Indore
Qualification: M.Tech. / M.Sc. / B.Tech. in Biotechnology / Microbiology / Biochemistry
Experience: 3–6 Years

Symbiotec – Downstream Production / R&D Department

Sr. Executive – Downstream

Vacancies: 07
Location: Ujjain / Indore
Qualification: M.Tech. / M.Sc. / B.Tech. in Biotechnology / Microbiology / Biochemistry
Experience: 6–10 Years

Symbiotec – Downstream Production / R&D Department

Assistant Manager – Downstream

Vacancies: 07
Location: Ujjain / Indore
Qualification: M.Tech. / M.Sc. / B.Tech. in Biotechnology / Microbiology / Biochemistry
Experience: 10–12 Years

Symbiotec – Quality Control Department

Executive – QC

Department: QC (IPQC / HPLC / Wetlab / GC)
Vacancies: 05
Location: Ujjain / Indore
Qualification: M.Pharm. / B.Pharm. / M.Sc. / B.Sc.
Experience: 3–6 Years

Sr. Executive – QC

Department: QC (IPQC / HPLC / Wetlab / GC)
Vacancies: 05
Location: Ujjain / Indore
Qualification: M.Pharm. / B.Pharm. / M.Sc. / B.Sc.
Experience: 6–10 Years

Symbiotec – Quality Assurance Department

Executive – QA

Department: QA (Validation, Qualification, IPQA, QMS)
Vacancies: 05
Location: Ujjain / Indore
Qualification: M.Pharm. / B.Pharm. / M.Sc. / B.Sc.
Experience: 3–6 Years

Sr. Executive – QA

Department: QA (Validation, Qualification, IPQA, QMS)
Vacancies: 05
Location: Ujjain / Indore
Qualification: M.Pharm. / B.Pharm. / M.Sc. / B.Sc.
Experience: 6–10 Years

Eligibility & Qualifications

Symbiotec – Upstream & Downstream

M.Tech. | M.Sc. | B.Tech. (Biotechnology / Microbiology / Biochemistry)

Symbiotec – QC & QA

M.Pharm. | B.Pharm. | M.Sc. | B.Sc.

Experience Requirements

Symbiotec – Upstream & Downstream

1–12 Years, depending on the position.

Symbiotec – QC

3–10 Years, depending on the position.

Symbiotec – QA

3–10 Years, depending on the position.

Walk-In Interview Details

Symbiotec – Vadodara Walk-In Drive

Date: 20th September 2026 (Sunday)
Time: 9:00 AM – 4:00 PM
Venue: Conference Hall, Hotel Fortune Inn Promenade
Address: 9 Pratham Avenue, Akota, Vadodara, Gujarat – 390020

How to Apply

Interested candidates can send their CVs to:

Email: jai.mirchandani@symbiotec.com
Email: vinita.sarkar@symbiotec.com

Symbiotec – Contact

Jai Mirchandani: +91 9630061862
Vinita Sarkar: +91 9630090603

Latest Date: 20th September 2026

Job Summary

APL Healthcare Limited, Unit 1, Jadcherla, is conducting a Walk-In Interview for Packing roles.
The opening is for TA / Executive positions in Primary and Secondary Packing operations.
Candidates with ITI, Diploma, or B.Pharmacy qualifications and 3–8 years of experience can apply.
The interview is scheduled for 19th September 2026, from 10:00 AM to 12:00 PM.

APL Healthcare Limited – Packing Department

TA / Executive – Packing

Department: Packing
Position: TA / Executive
Experience: 3–8 Years
Qualification: ITI / Diploma / B.Pharmacy

APL Healthcare Limited – Packing Role

Primary & Secondary Packing

The position covers packing activities involving:

• Bottle Packing
• Powder Filling
• Sachet Filling
• Primary Packing
• Secondary Packing

Eligibility & Qualifications

APL Healthcare Limited – Packing

ITI | Diploma | B.Pharmacy

Candidates should have 3–8 years of relevant experience in packing operations.

Experience Requirements

APL Healthcare Limited – TA / Executive

3–8 Years

Relevant experience in primary and secondary packing, bottle packing, powder filling, or sachet filling is applicable to the role.

Job Location

APL Healthcare Limited – Unit 1

APL Healthcare Limited, Unit 1, Jadcherla

The supplied recruitment poster identifies the work and interview location as APL Healthcare Limited, Unit 1, Jadcherla.

Walk-In Interview Details

APL Healthcare Limited – Packing Walk-In

Date: 19th September 2026 (Saturday)
Time: 10:00 AM – 12:00 PM

Documents to Carry

APL Healthcare Limited – Interview Documents

Candidates should carry:

• Updated Resume
• Academic Documents
• CTC Breakup
• Last 3 Months’ Payslips
• Bank Statement

How to Apply

Interested and eligible candidates can attend the walk-in interview at:

APL Healthcare Limited, Unit 1, Jadcherla

Candidates should carry the required documents and report during the scheduled interview time.

Job Summary

Finecure Pharmaceuticals Limited is conducting a Walk-In Interview in Ahmedabad for multiple positions across its pharmaceutical operations.
The openings cover Production, Production/Packing, Engineering, Quality Assurance, Quality Control, Microbiology, R&D, and SCM functions.
Experience requirements range from 0–6 years, depending on the position and department.
Candidates should attend the interview with their updated resume and required documents at the scheduled venue.

Finecure Pharmaceuticals – Production Department

Sr. Officer / Executive – Production

Experience: 2–6 Years

Finecure Pharmaceuticals – Production Skills

• Production
• Shift Management

Finecure Pharmaceuticals – Production / Packing Department

Operator – Production / Packing

Experience: 2–7 Years

Finecure Pharmaceuticals – Production / Packing Skills

• Granulation
• Compression
• Blister Packing
• Alu-Alu Packing

Finecure Pharmaceuticals – Engineering Department

Operator – Engineering

Experience: 1–4 Years

Finecure Pharmaceuticals – Engineering Skills

• Plant Maintenance
• HVAC Maintenance
• Electrical Maintenance
• Water System Operations

Finecure Pharmaceuticals – Quality Assurance Department

Officer / Sr. Officer – Quality Assurance

Experience: 2–5 Years

Finecure Pharmaceuticals – QA Skills

• IPQA
• QA
• AQA

Finecure Pharmaceuticals – Quality Control Department

Officer / Sr. Officer – Quality Control

Experience: 2–5 Years

Finecure Pharmaceuticals – QC Skills

• HPLC
• RM Analyst
• PM Analyst

Finecure Pharmaceuticals – Microbiology Department

Jr. Officer / Officer – Microbiology

Experience: 1–3 Years

Finecure Pharmaceuticals – Microbiology Skills

• MLT
• Environmental Monitoring

Finecure Pharmaceuticals – R&D Department

Jr. Officer / Officer – R&D

Experience: 1–3 Years

Finecure Pharmaceuticals – R&D Skills

• Formulation Development – OSD
• Documentation
• Coordination

Finecure Pharmaceuticals – SCM Department

Jr. Officer / Officer – SCM (Invoicing)

Experience: 0–2 Years

Finecure Pharmaceuticals – SCM Invoicing Skills

• Order Processing
• Invoicing
• Communication Skills

Finecure Pharmaceuticals – SCM PPIC Department

Jr. Officer / Officer – SCM – PPIC

Experience: 1–4 Years

Finecure Pharmaceuticals – PPIC Skills

• Production Planning
• Inventory Control
• Communication Skills

Eligibility & Qualifications

Finecure Pharmaceuticals – Educational Qualification

The recruitment poster does not specify minimum educational qualifications for the listed positions.

Candidates should therefore refer to the official recruitment communication or confirm the qualification requirements with the recruitment team before attending the interview.

Experience Requirements

Finecure Pharmaceuticals – Department-wise Experience

Production: 2–6 Years
Production / Packing: 2–7 Years
Engineering: 1–4 Years
Quality Assurance: 2–5 Years
Quality Control: 2–5 Years
Microbiology: 1–3 Years
R&D: 1–3 Years
SCM – Invoicing: 0–2 Years
SCM – PPIC: 1–4 Years

Walk-In Interview Details

Finecure Pharmaceuticals – Ahmedabad

Date: 20th September 2026 (Sunday)
Time: 09:00 AM – 03:30 PM

Interview Venue

1201-A, Mondeal Heights,
Near Iscon Circle, S.G. Highway,
Ahmedabad – 380015, Gujarat

Finecure Pharmaceuticals – Documents to Carry

Walk-In Interview Documents

Candidates should bring:

• Updated CV
• Educational Certificates
• Experience Certificates
• Passport-Size Photograph
• Latest Increment Letter / Salary Slip

How to Apply

Interested candidates can attend the walk-in interview at the venue with the required documents.

Candidates can also share their CV at:

Email: career@finecurepharma.com

Finecure Pharmaceuticals – Website

www.finecurepharma.com

Job Summary

Chemspec Chemicals Pvt. Ltd. is hiring an Officer / Sr. Officer – R&D for its research and development team.
The position is based in Taloja, Navi Mumbai and requires 2–5 years of experience in R&D.
Candidates should hold an M.Sc. in Analytical Chemistry with experience in Cosmetic Chemistry, Personal Care Molecule Development, or Specialty Ingredients.
The role involves chemical synthesis, analytical testing, pilot studies, technology transfer, stability studies, and R&D documentation.

Chemspec Chemicals – R&D Department

Officer / Sr. Officer – R&D

Position: Officer / Sr. Officer – R&D
Qualification: M.Sc. – Analytical Chemistry
Experience: 2–5 Years in R&D
Work Location: Taloja, Navi Mumbai
Reports To: R&D Manager

Chemspec Chemicals – Job Description

R&D – Responsibilities

• Chemical synthesis and chemical RM testing.
• Support pilot studies, literature surveys, documentation, analytical reviews, and other research laboratory activities.
• Conduct research activities for new and existing ingredients and finished products.
• Evaluation of raw materials, active ingredients, and preservatives.
• Conduct bench trials and pilot batches, including technology transfer.
• Stability, compatibility, and microbiological testing.
• Maintain R&D records and prepare BMR.
• Ensure regulatory compliance with FDA, BIS, and international requirements.
• Provide technical support to production and the pilot plant.
• Keep track of industry trends, sustainable technologies, and innovations.
• Perform other R&D-related functions assigned from time to time.

Chemspec Chemicals – Skills Required

R&D – Required Skills

• Strong research and analytical skills.
• Relevant expertise in Cosmetic Chemistry / Personal Care Molecule Development, including specialty ingredients.
• Hands-on experience with analytical laboratory instruments.
• Ability to multitask and work independently.
• Good communication and coordination ability.

Eligibility & Qualifications

Chemspec Chemicals – R&D

M.Sc. – Analytical Chemistry

Candidates should have relevant R&D experience along with exposure to Cosmetic Chemistry, Personal Care Molecule Development, and Specialty Ingredients.

Experience Requirements

Chemspec Chemicals – Officer / Sr. Officer – R&D

2–5 Years

The recruitment requirement specifically mentions R&D experience with experience in Cosmetic Chemistry / Personal Care Molecule Development & Specialty Ingredients.

Job Location

Chemspec Chemicals Pvt. Ltd.

Taloja, Navi Mumbai, Maharashtra

How to Apply

Interested candidates can share their updated CV at:

Email: h.pillai@chemspec.co.in
Email: shweta.mohite@chemspec.co.in

Candidates should mention the R&D position while applying.

Job Summary

Thermo Fisher Scientific Hiring – FSP CTC II | Clinical Trial Coordinator II

Thermo Fisher Scientific is hiring for FSP CTC II within its Clinical Research Services / PPD clinical research portfolio in Mumbai.
The role supports clinical trial teams with site activation, feasibility, document management, regulatory tracking, and trial coordination activities.
Candidates with a Bachelor’s degree preferred and at least 2 years of comparable Clinical Trial Coordinator (CTC) experience can apply.
Experience with Veeva eTMF, CTMS, global clinical trials, and coordination with local/global teams is specifically required.

Thermo Fisher Scientific – Clinical Research Department

FSP CTC II

Job ID: R-01367751
Job Type: Full-time
Location: Mumbai, Maharashtra, India
Work Mode: Fully Remote
Category: Clinical Research
Work Schedule: Standard (Monday–Friday)

Thermo Fisher Scientific – FSP CTC II Role

Clinical Trial Coordination

The FSP CTC II role provides administrative and technical support to clinical trial project teams and contributes to site activation, feasibility, documentation, tracking, and project delivery activities.

Thermo Fisher Scientific – Key Responsibilities

FSP CTC II – Clinical Trial Activities

• Coordinate, oversee, and complete assigned trial activities according to the applicable task matrix.
• Perform department, internal, country, and investigator file reviews and document findings in the relevant systems.
• Ensure assigned tasks are completed on time, within budget, and to the required quality standards.
• Communicate project risks proactively to project leads and the line manager.
• Process documents sent to the client eTMF and perform eTMF reviews.
• Support mass mailings, communications, and distribution of documents and reports to internal teams.
• Review and track local regulatory documents.
• Analyze and reconcile study metrics and findings reports.
• Support clarification and resolution of site documentation findings.
• Maintain vendor trackers.
• Assist with coordination, compilation, and distribution of Investigator Site File and Pharmacy binder materials and non-clinical study supplies.
• Support study-specific translation materials and translation quality control.
• Provide technical and administrative support in collaboration with internal departments and team members.
• Maintain knowledge of SOPs, client directives, regulatory guidelines, and applicable work practices.
• Ensure trial status information is accurately maintained in relevant databases.
• Maintain relationships with client local affiliates where applicable.
• Support Strategic Collaboration site inclusion in the process.
• Conduct onsite feasibility visits where applicable for Asia-Pacific activities.
• Train new personnel in processes and systems.
• Support study-specific documentation, systems, tools, trackers, training requirements, and system access management.
• Ensure the eTMF remains up to date according to scheduled file reviews.
• Provide system support for platforms such as Activate and eTMF where applicable.
• Support risk-based monitoring activities.
• Transmit documents to clients and centralized IRB/IEC where required.
• Attend Kick-Off Meetings and take meeting notes when required.
• Support scheduling and organization of client and internal meetings.
• Support site start-up activities and alignment with the site activation critical path.
• Assist with regulatory compliance review packages.
• Support regulatory submissions during study start-up where applicable.
• Obtain site-selection documents directly from sites when required.
• Develop and maintain site lists using internal and external sources.
• Maintain investigator and site staff contact information in company systems.
• Complete Site Interest Plans in CTMS and document site communications and follow-ups.
• Review survey data for completeness, logic, and relevance.
• Collaborate with clinical teams to meet project deadlines and resolve site issues.
• Maintain efficient plans for site contact and follow-up and escalate concerns where needed.
• Support local knowledge of site capacity and experience and contribute to site tiering.
• Conduct physician and site personnel interviews to support trial optimization projects.
• Liaise with Global Investigator Services to resolve investigator queries.
• Contribute to global strategic feasibility processes and best practices.

Thermo Fisher Scientific – Education & Experience

FSP CTC II – Eligibility & Qualifications

Bachelor’s Degree Preferred

Candidates should also have:

At least 2 Years of Comparable Clinical Trial Coordinator Experience

The source specifically requires previous CTC experience providing the knowledge, skills, and abilities needed to perform the role.

Thermo Fisher Scientific – Mandatory Experience

FSP CTC II – Required Systems Experience

• Veeva eTMF experience
• CTMS experience
• Experience working on global clinical trials
• Experience coordinating with local and global team members

Preferred Experience

Vendor Management experience is preferred.

Thermo Fisher Scientific – Required Skills

FSP CTC II – Professional Skills

• Ability to work independently or as part of a team.
• Strong organizational skills and attention to detail.
• Ability to manage multiple tasks efficiently.
• Strong project-data and systems analysis skills.
• Strong customer focus.
• Flexibility and adaptability when project priorities change.
• Knowledge of applicable country regulations.
• Knowledge of ICH Good Clinical Practices (GCP).
• Understanding of organizational and client SOPs and work practices.
• Excellent English language and grammar skills.
• Local language proficiency as required.
• Good presentation skills.
• Strong MS Office skills, including Word, Excel, and PowerPoint.
• Ability to learn and use clinical trial database systems.
• Effective oral and written communication skills.
• Strong interpersonal and negotiation skills.
• Basic medical terminology and therapeutic area knowledge.
• Basic organizational and planning skills.
• Basic knowledge of local health systems.
• Ability to manage risks and escalate issues appropriately.
• Ability to work effectively in a matrix environment.
• Relationship-building skills and independent thinking.

Thermo Fisher Scientific – Clinical Research Knowledge

FSP CTC II – Regulatory & Clinical Skills

The role requires the ability to maintain working knowledge of:

GCP | Applicable SOPs | Country Regulations | Clinical Trial Processes | Medical Terminology | Site Activation | Feasibility | Regulatory Documentation

Thermo Fisher Scientific – Working Conditions

FSP CTC II – Work Environment

The position may involve work in:

• Office environment
• Laboratory environment
• Clinical environment
• Home-office environment

The role may also require occasional drives to site locations and occasional travel.

Job Location

Thermo Fisher Scientific – Mumbai

Mumbai, Maharashtra, India

Work Mode: Fully Remote

How to Apply

Interested and eligible candidates can apply through the official Thermo Fisher Scientific careers portal.

Official Job: Apply for FSP CTC II – Thermo Fisher Scientific

Job Summary

Hetero Biopharma Limited is conducting a Walk-In Drive for API Units for freshers across multiple departments.
The openings are available in Quality, Production, SMT-Intermediate, and Engineering functions for candidates meeting the specified age and qualification criteria.
Candidates from the 2024 to 2026 batches are eligible, with the age limit set at 18–26 years.
Selected candidates will work at Hetero Biopharma Hyderabad Units and may receive benefits including PF, ESI, medical insurance, subsidized food, and transportation.

Hetero Biopharma – Quality Department

Quality – M.Sc. Chemistry Candidates

Qualification: M.Sc. Chemistry – Organic / In-Organic / Analytical

Eligibility: 2024 to 2026 batches
Age Criteria: 18–26 Years

Hetero Biopharma – Production Department

Production – B.Pharm / B.Sc / B.Com / B.A Candidates

Qualification: B.Pharmacy / B.Sc. / B.Com. / B.A.

Eligibility: 2024 to 2026 batches
Age Criteria: 18–26 Years

Hetero Biopharma – SMT Intermediate Department

SMT – Intermediate Candidates

Qualification: MPC / BPC

Eligibility: 2024 to 2026 batches
Age Criteria: 18–26 Years

Hetero Biopharma – Engineering Department

Engineering – ITI Candidates

Qualification: ITI – Fitters / Electricians

Eligibility: 2024 to 2026 batches
Age Criteria: 18–26 Years

Hetero Biopharma – Eligibility & Qualifications

Hetero Biopharma – Quality

M.Sc. Chemistry | Organic Chemistry | Inorganic Chemistry | Analytical Chemistry

Hetero Biopharma – Production

B.Pharm | B.Sc | B.Com | B.A

Hetero Biopharma – SMT Intermediate

MPC | BPC

Hetero Biopharma – Engineering

ITI – Fitter | ITI – Electrician

Hetero Biopharma – Age & Batch Eligibility

Age Criteria

18–26 Years Only

Eligible Passout Batches

2024 | 2025 | 2026

Hetero Biopharma – Job Location

Hyderabad API Units

The selected candidates will work at Hetero Biopharma Hyderabad Units.

Hetero Biopharma – Employee Benefits

Benefits

• PF
• ESI
• Medical Insurance
• Subsidized Food
• Transportation

Hetero Biopharma – Walk-In Interview Schedule

22 September 2026

Venue: Giriraj Govt Degree College
Location: Gurubabadi, Nizamabad

24 September 2026

Venue: Siddhartha Degree & PG College
Location: Ramgiri, Nalgonda

30 September 2026

Venue: KNM Degree College
Location: Miryalaguda, Nalgonda

5 October 2026

Venue: Govt Degree College
Location: Kondangal, Vikarabad

Documents to Carry

Hetero Biopharma – Walk-In Documents

Candidates should carry:

• Updated Resume
• Educational Documents
• Aadhaar Card
• PAN Card
• Bank Passbook Xerox

How to Apply

Interested and eligible candidates can apply by scanning the QR code provided in the recruitment advertisement.

Candidates should carry the required documents and attend the walk-in interview at the applicable venue.

Hetero Biopharma – Application Email

Email: venumadhav.k@hetero.com

Job Summary

Credence Global Solutions Hiring – Executive Medical Coding | Ambulance Coding

Credence Global Solutions is hiring Executive – Medical Coding professionals for its Operations team.
The role is focused on US healthcare coding, with specific experience in Ambulance Coding required for the position.
Candidates should have at least 2 years of relevant experience and hold a CPC certification.
The position is based in Pune Kharadi and involves rotational shifts.

Credence Global Solutions – Medical Coding Department

Executive – Medical Coding

Department: Operations
Specialization: Ambulance Coding
Location: Pune Kharadi
Experience: Minimum 2 Years in US Healthcare Coding
Certification: CPC
Shift: Rotational

Credence Global Solutions has healthcare RCM operations serving healthcare providers, including medical transport providers and other healthcare organizations.

Credence Global Solutions – Medical Coding Responsibilities

Ambulance Coding – Job Responsibilities

• Work on the US Healthcare Coding Process.
• Handle Ambulance Coding assignments.
• Apply strong knowledge of ICD-10 and CPT-4 codes.
• Review complete medical records and identify the correct ICD-10 and procedure codes.
• Ensure selected codes support medical necessity.
• Identify and manage issues related to upcoding and downcoding.
• Apply correct sequencing for ICD-10 and procedure codes.
• Perform required activities on the legacy application and document memos.
• Work with the team to achieve project targets established by project leaders.
• Support project deliverables and take additional responsibility when required.

Credence Global Solutions – Eligibility & Qualifications

Executive – Medical Coding

CPC Certification – Mandatory

Candidates should have:

Minimum 2 Years of US Healthcare Coding Experience | Ambulance Coding Experience | Strong ICD-10 Knowledge | CPT-4 Knowledge

The official job description specifically requires previous experience in ambulance coding and CPC certification.

Credence Global Solutions – Experience Requirements

Medical Coding – Ambulance Coding

2+ Years

Relevant experience in US Healthcare Coding is required, with prior Ambulance Coding experience.

Credence Global Solutions – Key Skills

Medical Coding Skills

• ICD-10 coding
• CPT-4 coding
• Medical record review
• Medical necessity assessment
• Code sequencing
• Ambulance coding
• Upcoding and downcoding awareness
• US healthcare coding processes

Shift Details

Credence Global Solutions – Medical Coding

Rotational Shift

Job Location

Credence Global Solutions – Pune

Pune Kharadi, Maharashtra

Credence lists Pune, India among its delivery office locations.

How to Apply

Interested candidates can share their updated CV at:

Email: mansi.sonawane@in.credencerm.com

Candidates should mention Medical Coding – Ambulance Coding while applying.

Recruitment Notice

Credence Global Solutions – Hiring Process

Credence states that it does not charge any fees at any stage of recruitment and does not authorize third parties or individuals to request money in exchange for employment.

For recruitment-related concerns, the official HR contact listed in the source is hr@credencerm.com.

Job Summary

Meghmani Organics Ltd. is hiring professionals across Analytical Chemistry, Document Control Office, and Archivist functions.
The openings are available for Chemist, Officer, Assistant Manager, and Chemist/Officer positions with experience ranging from freshers to 12 years.
Candidates with B.Sc. and M.Sc. qualifications can apply for the relevant roles.
The opportunities are based at Chharodi, Ahmedabad, and the recruitment notice specifies male candidates only.

Meghmani Organics – Analytical Chemistry Department

Chemist – Analytical Chemistry

Vacancies: 2
Qualification: B.Sc. / M.Sc.
Experience: Fresher to 2 Years

Meghmani Organics – Chemist Responsibilities

• Handling basic analytical instruments such as Analytical Balance, pH Meter, Melting Point Apparatus, Karl Fischer, and moisture analyser.
• Communication skills in English.
• Proper documentation.

Officer – Analytical Chemistry

Vacancies: 1
Qualification: B.Sc. / M.Sc.
Experience: 3–4 Years

Meghmani Organics – Officer Responsibilities

• Handling basic analytical instruments.
• Experience with HPLC, GC, and other analytical instruments such as pH Meter, Melting Point Apparatus, and Karl Fischer moisture analyser.
• Communication skills in English.
• Proper documentation.
• Knowledge of OECD principles of GLP is preferable.

Assistant Manager – Analytical Chemistry

Vacancies: 1
Qualification: M.Sc.
Experience: 10–12 Years

Meghmani Organics – Assistant Manager Responsibilities

• Handling advanced analytical instruments including HPLC, GC, LC-MS, GC-MS, FTIR, and other high-end instruments.
• Interpretation of analytical results and characterization data using LC-MS, GC-MS, FTIR, and NMR.
• Strong knowledge of analytical method development and validation.
• Troubleshooting and laboratory management to deliver output within the required timelines.
• Communication skills in English and proper documentation.
• Knowledge of OECD principles of GLP is preferable.

Meghmani Organics – Document Control Office

Chemist – Document Control Office

Vacancies: 2
Qualification: B.Sc. / M.Sc.
Experience: Fresher to 2 Years

Meghmani Organics – Document Control Profile

The job role is similar to the Chemist – Analytical Chemistry position.

Meghmani Organics – Archivist Department

Chemist / Officer – Archivist

Vacancies: 2
Qualification: B.Sc. / M.Sc.
Experience: Fresher to 2 Years

Meghmani Organics – Archivist Responsibilities

• Manage proper indexing and safe storage of documents and samples.
• Job role is similar to the Chemist position.

Eligibility & Qualifications

Meghmani Organics – Analytical Chemistry

B.Sc. | M.Sc.

Meghmani Organics – Assistant Manager

M.Sc.

Meghmani Organics – Document Control Office

B.Sc. | M.Sc.

Meghmani Organics – Archivist

B.Sc. | M.Sc.

Experience Requirements

Meghmani Organics – Chemist

Fresher to 2 Years

Meghmani Organics – Officer

3–4 Years

Meghmani Organics – Assistant Manager

10–12 Years

Meghmani Organics – Document Control Office

Fresher to 2 Years

Meghmani Organics – Archivist

Fresher to 2 Years

Important Recruitment Note

Meghmani Organics – Candidate Preference

Male candidates only as specified in the recruitment advertisement.

Candidates should also mention the position they have applied for while submitting their application.

Job Location

Meghmani Organics Ltd.

Chharodi, Ahmedabad, Gujarat

How to Apply

Interested candidates can send their CV through LinkedIn Direct Message or email their updated resume to:

Email: prarthana.shah@meghmani.com

Candidates should clearly mention the position applied for in their application.

Job Summary

Granules Life Sciences is conducting a Walk-In Interview for multiple manufacturing and quality roles in Hyderabad.
The openings are available in Production, Packing, Engineering, and Quality Assurance (IPQA) departments.
Candidates with 3–5 years of experience can apply for Operator roles, while the IPQA Officer position requires 1–3 years of experience.
Immediate joiners, candidates willing to work in all shifts, and professionals with relevant technical contract manufacturing experience are encouraged to apply.

Granules Life Sciences – Production Department

Operator – Production

Experience: 3–5 Years

Granules Life Sciences – Production Skills

• Compression
• Granulation
• Ohara Coating
• Capsule Filling / Press Fit

Granules Life Sciences – Production Machines

• Korsch XT600
• Fette
• ACG 1800 & 1500

Granules Life Sciences – Packing Department

Operator – Packing

Experience: 3–5 Years

Granules Life Sciences – Packing Skills

• Bottle Packing
• Blister Packing

Granules Life Sciences – Packing Machines

• Uhlmann
• IMA
• Cartonator
• Pharmapack
• Bottle Counting Machine
• Sensum

Granules Life Sciences – Engineering Department

Operator – Engineering

Experience: 3–5 Years

Granules Life Sciences – Engineering Skills

• Well-versed in equipment maintenance knowledge related to FBP, Compression, Capsules, Blister and Bottle packing lines.
• Preventive and breakdown maintenance troubleshooting.
• Root Cause Analysis (RCA) for process equipment.
• Preventive maintenance as per schedule.
• Follow safety, SOP and cGMP requirements.

Granules Life Sciences – Quality Assurance Department

Officer – Quality Assurance (IPQA)

Experience: 1–3 Years

Granules Life Sciences – IPQA Skills

• In-process Quality Assurance
• Sampling & Testing
• Documentation & Records
• Process Compliance
• GMP / cGMP Norms

Eligibility & Qualifications

Granules Life Sciences – Production Operator

Qualification: Not specified in the recruitment poster.

Candidates with relevant pharmaceutical production experience in compression, granulation, coating, and capsule filling can apply.

Granules Life Sciences – Packing Operator

Qualification: Not specified in the recruitment poster.

Relevant pharmaceutical packing experience is preferred.

Granules Life Sciences – Engineering Operator

Qualification: Not specified in the recruitment poster.

Relevant engineering or technical manufacturing experience is applicable to the role.

Granules Life Sciences – IPQA Officer

Qualification: Not specified in the recruitment poster.

Candidates with relevant pharmaceutical quality assurance experience can apply.

Experience Requirements

Granules Life Sciences – Production Operator

3–5 Years

Granules Life Sciences – Packing Operator

3–5 Years

Granules Life Sciences – Engineering Operator

3–5 Years

Granules Life Sciences – IPQA Officer

1–3 Years

Granules Life Sciences – Candidate Preferences

Hiring Preferences

• Immediate joiners are preferred.
• Candidates should be willing to work in all shifts.
• Attractive remuneration is offered based on experience and skills.
• Candidates currently working in Technical Contract Services with formulation or production experience are also eligible.

Walk-In Interview Details

Granules Life Sciences – Walk-In Interview

Date: 26th September 2026 (Saturday)
Time: 10:00 AM – 02:00 PM
Venue: VR Ashoka Grand, Miyapur, Hyderabad

Job Location

Granules Life Sciences

Shamirpet, Hyderabad – 500101

How to Apply

Interested candidates can attend the Granules Life Sciences Walk-In Interview at the above-mentioned venue with their updated resume.

Candidates should be prepared for the relevant Production, Packing, Engineering, or IPQA position based on their experience and skills.

Job Summary