Immacule Life Sciences – Mega Walk-In Interviews for QA / QC / Production / Packing / Engineering on 16th Sep’ 2023

Immacule Lifesciences is the fastest growing One Stop Solution for Injectable, from Development to commercial manufacturing of injectable in liquid in aqueous/non aqueous as well as in Lyophilized dosage forms in vial and ampoules in non-oncology space with robust capabilities for terminal sterilization as well as aseptically filled injectable.

With a global footprint across countries, including the United States, Europe, Australia and other emerging markets, we are backward integrated in the pharmaceutical research and development alongside manufacturing complex injectables.

We are now seeking potential and talented individuals who possess the right aptitude and attitude to join our injectable facility based at Nalagarh.

The Walk-in Drive have been scheduled as follows:

Excellent opportunity in Pharmaceutical Industry at Nalagarh

Department: QA / QC / Production / Packing / Engineering

Designation: Executive / Officer / Operator

Qualification: B.Pharm, M.Pharm, M.Sc, B.Sc, B.Tech, D.Pharm, Diploma, ITI, 12th

Experience: 1 to 8 yrs

Job Location: Nalagarh

Walk-In Interview Details:

Date: 16th September, 2023 (Saturday)

Time: 9:30 AM to 4:00 PM

Venue: Immacule Lifesciences Pvt. Ltd.

Village Thanthewal, Ropar Road, Nalagarh, Solan (HP) – 174101, India

Job Description: 

Production/Packing (Sterile):- Executive/Sr. Officer/Officer

Qualification : B. Pharma/ M. Pharma

Experiences : 01 to 08 Years

Skills :Good Knowledge of Washing & Tunnel Manufacturing/ Liquid Vial and ampoule filling /Sealing/Autoclave/TS/ /Lyo. /Track & Trace/ Visual Inspection & Packing.

Production/Packing (Sterile):- Operator/Technician

Qualification : ITI/Diploma/D. Pharma

Experiences : 02 to 08 Years

Skills :Good Knowledge of Washing & Tunnel Manufacturing/ Liquid Vial and ampoule filling /Sealing/Autoclave/TS/ /Lyo. /Track & Trace/ Visual Inspection & Packing

Quality Assurance (Sterile): Executive/Sr. Officer/Officer

Qualification : B. Pharma/ M. Pharma/ M.Sc

Experiences : 01 to 08 Years

Skills :Good Knowledge of Qual. & Validation/ QMS/Documentation/ Training/ IPQA/AQA/ Audit & Compliance

Quality Control (Sterile): Executive/Sr. Officer/Officer

Qualification : B. Pharma/ M. Pharma/ M.Sc

Experiences : 01 to 08 Years

Skills :Should have operation knowledge of HPLC, GC, Dissolution, GLP/RM/FG/Stability

QC Microbiology (Sterile): Executive / Sr. Officer / Officer

Qualification : M.Sc Micro

Experiences : 02 to 08 Years

Skills :Good Knowledge of EM/GPT/Media Preparation/Water / GLP/ Bioburden /Culture.

Engineering (Sterile): Executive / Sr. Officer / Technician

Qualification : B. Tech/Diploma/IT

Experiences : 02 to 08 Years

Skills :Good Knowledge of Injectable Process Equipment/ Utility/HVAC/ Water System/Chiller/Boiler .

Interested candidates from Injectable Background may attend walk-in interviews with a copy of resume, CTC break up.

Note: Candidates already appeared for an interview within the last 06 months, will not be eligible for the interviews.

Those who are unable to attend Walk In may send their updated resume with the details of total experience, current CTC, expected CTC & notice period on career@acmeformulation.com

Please note that Immacule Lifesciences does not hire consultants/agents who promise interviews/jobs for monetary consideration/registration fees. Beware of such fraudulent calls.

BDR Pharmaceuticals – Urgent Openings for Production / QC / Packing / Warehouse Departments – Apply Now

BDR Pharmaceuticals was Established in 2002 into API manufacturing, we have a consolidated position in the domestic and global market for the API Business. In today’s dynamic global pharmaceutical market, we at BDR Pharmaceuticals have carved a niche for ourselves, with our formulations portfolio for specialty medication. Our unique strategy of multi-branding ensures that critical and lifesaving medicines are available at affordable prices with two API and formulation facilities at Gujarat, Uttarakhand and a pellet facility at Hyderabad. BDR PHARMACEUTICALS INTERNATIONAL PVT. LTD. SURVEY NO-51/1/2.51/2,52/2/1,52/2,54/2 AT-VANSETI VILLAGE PO-TAJPURA, HALOL, VADODARA, GUJARAT.

We are hiring Multiple Openings in below following positions.

Department: Production / QC / Packing / Warehouse

Designation: Officer / Sr. Officer / Technician Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm

Experience: 2-8 yrs 

Location: Vadodara, Gujarat

Interested Candidates can Forward their CV on roshni.makkad@bdrpharma.com 

Alkem Laboratories – Walk-In Interviews on 17th Sep’ 2023 for QC / QA / Production / Engineering

Alkem Laboratories Limited is an Indian multinational pharmaceutical company headquartered in Mumbai, Maharashtra, India that manufactures and sells pharmaceutical generics, formulations and nutraceuticals in India and globally. We are a leading Indian pharmaceutical company with global operations, engaged in the development, manufacture and sale of pharma & nutraceutical products.

Alkem Laboratories Ltd is Conducting Walk-In Interview for Our Formulation Manufacturing Facility based at Daman. Walk-In Interview for Experienced in Quality Control – Formulations on 17th Sep’ 2023 at Indore.

JOB DESCRIPTION

Department: Quality Control, Quality Assurance Division: Formulation

Qualification: B.Pharm, M.Sc, B.Sc

Position: Executive / Officer / Sr. Executive / Sr. Officer

Experience: 1 to 10 years

Job Location: Daman

Documents Required:

Copy of your resume, Latest copies of results, Passport size photograph, Copy of Aadhaar & PAN Card.

 

WALK-IN INTERVIEW DETAILS:

Date: 17th Sep’ 2023 (Sunday)

Time: 09:00 AM to 04:00 PM

Venue: Hotel Red Maple Mashal, Rasalpura, Rau, Indore, Madhya Pradesh – 453446

Quality Control – Area of Expertise

1. RM/FG & Stability / Analytical Instrumentation-HPLC, UV and Dissolution.

2. Handling of LIMS, Empower, SAP will be preferable.

3. Regulatory knowledge & 21 CFR part 11 understanding is must.

Quality Assurance – Area of Expertise

1. IPQA (Mfg. & Packing), shop floor activities. Should have exposure of regulatory audits.

2. ITQA Audit trail review and computer system, server & IPC/SCADA system verification.

3. CSV & Equipment Qualification Section

Documents Required:

Copy of your resume, Salary breakup/Increment letter, Passport size photograph, Copy of Aadhaar & PAN Card.

Note: Throughout 50% and above required in academics.

JOB DESCRIPTION:

Department: Production / Engineering

Qualification: B.Pharm, M.Pharm, ITI, Diploma

Position: Executive / Officer / Sr. Executive / Sr. Officer

Experience: 3 to 10 years

Job Location: Baddi

Documents Required:

Copy of your resume, Salary breakup/Increment letter, Passport size photograph, Copy of Aadhaar & PAN Card.

 

Contact: 01795-668999. Extension 207, 8628099881

Mail – hrbaddi@alkem.com

Venue: Hotel Red Maple Mashal, Rasalpura, Rau, Indore, Madhya Pradesh – 453446

Exemed Pharmaceuticals – Openings in QC / QA / R&D / ADL – Apply Now

Exemed Pharmaceuticals is a young business with ambitious growth goals, We currently hold GMP certification from both the WHO and the EU. We are seeking young, enthusiastic, and ambitious professionals for the following positions in light of our planned expansion in OSDI at our Vapi facility.

Required Quality Control- Officer / Sr. Officer / Executive

Job description (JD):

Experience: 1-5 yrs

Qualification: Masters (Chemistry)

Candidate should have following criteria:

Experience of 1-6years in Quality Control.

Handling instruments like HPLC and GC-Headspace.

Handling other analytical instruments like KF-Titrator, Auto-Titrator, pH-meter, Polarimeter, UV Spectrophotometer, Balance etc.

Analysis of In-process monitoring, Raw material, Intermediates, Stability studies and Drug substances (API).

Analytical method development and analytical method validation exposure.

Calibration of analytical instruments

Should follow GLP practices, Document preparation for Specifications, SOPs, Certificate of analysis and technical reports.

Email : hr@exemedpharma.com

Executive / Senior Executive -Quality Assurance

Experience: 7-12 yrs

Job Responsibility:

To Review of Equipment, Instruments qualifications activities i.e. Protocol, Report execution.

To prepare and review of Process Validation Protocol/reports, cleaning validation protocols, reports related study.

Engineering related Compliances and including drawing list updation.

To prepare and review of Risk Assessment for facility and product.

To review, issue & closure of QMS documents i.e. Change Control, Deviation, OOS, OOT, CAPA, Market complaints etc.

To review new master BMR/ECR.

To review APQR and PQR for MFH and Allopurinol USP, CEP and ROW and to ensure data updated regulated.

Responsible for approve or reject intermediate & Bulk and to release finished product batches.

Responsible for the Document archival room management.

Responsible for Transport validation activity.

Responsible for Documentation for FDA & WHO for renewal or new license applications.

In charge of IPQA team (Sampling, Labeling and Control sample)

To perform internal audit (Self inspection)/external audits and provide compliance report for internal/external audits.

To prepare and review the SOPs as per SOP on SOP.

To Review PTD, Technology transfer documents as per SOP for new products.

To ensure GMP compliances in Facility.

Responsible for initiation, compilation of activities required as per respective SOPs.

Responsible to ensure and carry out proper document correction and writing procedure.

To verify preventive maintenance & calibration activities performed of all equipment & measuring instruments in the manufacturing plant.

Responsible for preparation & review of VMP & SMF.

Responsible to verify the technical documents of manufacturing and R & D.

Responsible for the regulatory and customer correspondence.

To review SOPs, STPs, specifications and GTPs.

Responsible for Stability summary report Approval.

To Review Batch Manufacturing Records, Batch Processing Records, Equipment Cleaning Records, Process Development Reports.

To prepared, Review and Approved COA.

Responsible to maintain reconciliation of the product labels, Approved label and seal in the respective logs.

Responsible for return and recall of materials and also for mock recall activities.

Responsible for preparation of Organogram of personnel in departments.

Responsible sampling activities as per SOP,

To review of Method Validation Protocols & Reports.

Responsible for the review of the stability study protocol, sample charging in stability study and withdrawal of samples, stability study report review and summary report preparation.

Responsible for the issuance, distribution, and retrieval of SOPs and logbooks.

Responsible for the issuance, retrieval and review of BMR, BPR, ECR, SRR and other processing documents, to provide batch numbering as per SOP.

Responsible for the control sample management and document control activities.

To ensure Standard Operating Procedures followed and displayed in the plant.

To co-ordinate during finished product dispatch.

Responsible for other activities as instructed by Head-QA whenever required.

Email : hr@exemedpharma.com

Required ADL Officer / Sr. Officer – Pharma API (Vadodara)

Company Name: Exemed Pharmaceuticals

Location: Luna/Ekalbara

ADL Officer / Sr Officer

Education: MSc Organic or Analytical Chemistry

Experience: 2 to 5 years experience in API Industry only.

Candidate must have:

Knowledge of method validation by HPLC and GC

Knowledge of ICPMS method development and method validation Knowledge of how to review analytical documents

Interested candidate may share updates resume on recruitment@exemedpharma.com

Urgently required Research Officer / Chemist / Associate for our company based at Ekalbara / Luna Vadodara) Location.

If interested & ready to relocate please share updated resume on recruitment@exemedpharma.com

Position :- Research Officer/Chemist /Associate

Department:- R&D Synthesis

Qualification:- M.Sc. (Chemistry/Organic Chemistry)

Experience:- 1-5years of relevant experience

Location :- Vadodara Key Skills and Competencies: -Experience in Organic Synthesis / Multi-step Synthesis.

Job Description:-

1. Process Development

2. Handling reactions from mg to gram scale.

3. Sound Knowledge of isolation, separation & purifications techniques.

4. Experience in characterization and identification of Organic molecules using spectroscopy techniques like NMR, IR, LCMS, HPLC.

5. Positive and confident individual with strong work ethics.

6. Team player and good communications skills.

7. Good Exposures in Organic Synthesis.

If interested & ready to relocate please share updated resume on recruitmemt@exemedpharma.com

 

Gufic Biosciences Limited – Urgent Openings for QC / QA / QC-Micro / Warehouse / Stores – Apply Now

Gufic Biosciences Limited of industries is a fastest growing and leading company in Lyophilization injection, API facility. Gufic Biosciences Limited having accreditation of WHO and EU GMP. We are having below vacancies for Navsari (Gujarat) Plant. We, Gufic Biosciences Ltd is a leading Pharmaceutical company in Lyophilization injection at Navsari (Gujarat) and having accreditation of WHO and EU GMP PPB Kenya, Uganda, Ukraine, Canada etc.

Hiring for below positions for formulation plant.
Company- Gufic Biosciences Limited .
Department:- Warehouse/ stores

• Designation- Officer/operator
• Location- Pithampur, Indore
• Education- ITI/B.Sc/diploma
• Experience- 2-6 Years

Job Profile:

• Must have experience of working in formulation plant.
• well versed with receipts and dispensing .
• handling day to day activities of warehouse
• material handling and verification
• dispatch of FG.
• experience of handling miscellaneous store.

Share resume on pushpendra.singh@guficbio.com , ajay.songara@guficbio.com and deepak.pathak@guficbio.com
candidates will have to join immediately or within 15 days

Hiring for Quality Assurance (Validation & Qualification ) for sterile injectable Plant!!!
Candidates must have working experience of Sterile / parenteral / Injectable Plant.
Company- Gufic Biosciences Ltd.
Designation- QA – Officer /Sr. Officer

• Location- Pithampur, Indore
• Education- B.Pharm
• Experience- 1-5 Years
• Process/Cleaning Validation
• Equipment Qualification
• Preparation of Protocol, URS, & other documents for IQ, OQ, PQ

Hiring QC officer/sr. officer
Company- Gufic Biosciences Ltd.

• Designation- officer/sr. officer
• Location- Pithampur, Indore
• Education- M.Sc chemistry
• Experience- 1-6 Years

Share resume on vinay.nimbola@guficbio.com and deepak.pathak@guficbio.com
Note:- Candidates have to join immediately or in 15 days

Hiring QC Microbiology officer / Sr. officer

• Company- Gufic Biosciences Ltd.
• Designation- officer / sr. officer
• Location- Pithampur, Indore
• Education- M.Sc (Micro/biotechnology )
• Experience- 1-6 Years – MLT, BET, Sterility, Environment Monitoring

Share resume on rajeev.sahu@guficbio.com and deepak.pathak@guficbio.com

 

Ami Lifesciences Walk In On 17th Sept’ 2023

Ami Lifesciences was founded with the goal of changing the way in which quality medicines are delivered to people in need. We operate on the principle by extending our focus and services to maximize our impact on the global pharmaceutical industry. We have spent last two decades in building up our scientific and technological capabilities, research, and manufacturing competencies. Along the way we have earned a reputation for being innovative, inventive and resourceful. We have built long term business association pharmaceutical companies of the world.

Ami Lifesciences Walk In

• Qualification: B.Tech/B.E,M.Tech in Chemical
• Experience : 02-05+years
• Department: Production 
• Role: Officer / Executive
• Job Location: Vadodara
• No.of Openings: 01
• Salary: 3.5-6.5 Lacs P.A.

Time and Venue:

17th September , 9.30 AM – 5.30 PM

2nd Floor, Productivity House, Baroda Productivity Road, Alkapuri, Vadodara – 390007

Contact – Aparna Mishra 

Job description:

• Responsible for production as per received plan and align for necessary equipment, raw material, and manpower with concerned departments.

• Responsible for allocation of Manpower and distribution of work.
• Submission of Daily Production Report in determined format (Input-Output Data, WIP, Stock Statement)
• Monitoring and ensuring cGMP activities and adhering to QMS.
• Planning and ensuring proper documentation like Change Control, CAPA, BPCR, OOS, OOT reports, internal and external audit compliance reports, etc.
• Planning of Preventive Maintenance, Breakdown Maintenance of equipment with line clearance.

Preferred candidate profile

• Candidate must posses BE/B.tech in chemical.
• Experience: 4 to 8 years of experience in Pharmaceuticals, API In pilot plant

IPCA Laboratories Limited Released Multiple Job Openings in Production & QC Dept

Ipca Laboratories Limited is an international pharmaceutical company based in Mumbai, India. Ipca sells these APIs and their intermediates world over. Ipca Laboratories Ltd is a fully integrated pharmaceutical company engaged in the manufacturing, marketing and distribution of Active Pharmaceutical Ingredients, pharmaceutical formulations and medicinal products across the globe. 

Ipca Laboratories Limited job vacancy

• Qualification: B.Sc,M.Sc, BE/B.Tech
• Experience : 03-05+years
• Job Location: Maharashtra
• No.of Openings: 06
• Department: Production,QC
• Position:- Sr. Officer/ Officer/ Sr.Executive

Contact Person Name & No. :-Mr. Kaustubh/Mr. Nihal (8767824323/9049473110)

Location Address:- Ipca Laboratories Ltd (Unit II) API, Plot no- E41,E128/2, E129, MIDC Tarapur, Boisar, Palghar, 401506, Maharashtra, India.

Job description