45 Gdp Jobs - Page 2

Department: Pharma Standard - AD Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. For Preparative: Experience on instruments like Preparative HPLC and SFC Expertise in Purification of peptides, impurity isolation. For Analytical: Expertise Analytical Method Development of peptides and oligoes. Regular sample analysis for supporting to synthesis team. Handling experience on DAC column packer and media packing will be advantageous. Department: Pharma Standard - Quality Control Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. Theoretical knowledge and hands-on experience on instruments like Shimadzu HPLC with Lab solution software, Agilent HPLC, Balance, pH meter, TGA instrument, FTIR. CGMP,GMP, experience on LCMS is preferrable. Knowledge on Data Integrity, GDP, QMS. Department: Pharma Standard - Inventory Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. Management of Inventory items, handling, weighing, dispatching of inventory materials. Hands-on experience on semi-microbalance, microbalance. Maintaining Real time stock updation of the inventory list in excel or SAP system and updating the stock quantities to the relevant stakeholders, whenever required. Basic understanding on Data Integrity, GDP and QMS Please bring your Updated CV along with last 3 Months Payslips, Recent Increment Letter, Aadhar Card/PAN Card: Date : Saturday, 10 May 2025 Time: 09:00 AM to 4:00 PM Walk-in Interview Location: Daicel Chiral Technologies (India) Pvt Ltd Genme Valley, IKP Knowledge Park, Survey No. 542/2, Koltur Village, Shamirpet Mandal, Medchal-Malkajgiri District, Hyderabad-500101 Note: Candidates who are unable to walk-In, May send their resume to hr@chiral.daice.com or whatsApp to 9000066897

Department: Pharma Standard - AD Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. For Preparative: Experience on instruments like Preparative HPLC and SFC Expertise in Purification of peptides, impurity isolation. For Analytical: Expertise Analytical Method Development of peptides and oligoes. Regular sample analysis for supporting to synthesis team. Handling experience on DAC column packer and media packing will be advantageous. ************************************************************************************************** Department: Pharma Standard - Quality Control Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. Theoretical knowledge and hands-on experience on instruments like Shimadzu HPLC with Lab solution software, Agilent HPLC, Balance, pH meter, TGA instrument, FTIR. CGMP,GMP, experience on LCMS is preferrable. Knowledge on Data Integrity, GDP, QMS. ************************************************************************************************** Department: Pharma Standard - Inventory Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. Management of Inventory items, handling, weighing, dispatching of inventory materials. Hands-on experience on semi-microbalance, microbalance. Maintaining Real time stock updation of the inventory list in excel or SAP system and updating the stock quantities to the relevant stakeholders, whenever required. Basic understanding on Data Integrity, GDP and QMS Please bring your Updated CV along with last 3 Months Payslips, Recent Increment Letter, Aadhar Card/PAN Card: Date : Saturday, 10 May 2025 Time: 09:00 AM to 4:00 PM Walk-in Interview Location: Daicel Chiral Technologies (India) Pvt Ltd Genme Valley, IKP Knowledge Park, Survey No. 542/2, Koltur Village, Shamirpet Mandal, Medchal-Malkajgiri District, Hyderabad-500101 Note: Candidates who are unable to walk-In, May send their resume to hr@chiral.daice.com or whatsApp to 9000066897

Preferred candidate profile Looking for a candidate with 2 to 4 years of work experience as QC analyst /AQA reviewer in reputed pharma companies. Should have Knowledge of handling/analytical data review of HPLC, FTIR, UV spectrophotometer, KF Autotitrator, Dissolution apparatus. Have Basic knowledge of CGMP, GDP, Data integrity. Should have Basic knowledge of OOS (Out of specification), OOT (Out of rend), OOC (Out of calibration).

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety, and quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces

QC Manager/ Sr. Manager Job Responsibilities Training to staff for following practices as per standard operating procedure, Good Laboratory Practices and Pharmacopoeia / in-house method of analysis To monitor data integrity in Compliance of good laboratory practice and Compliance of GMP in the Quality Control Laboratory. To check and sign Certificate of Analysis (COA) for export as well as domestic. To review and ensure Deviation, Corrective action Preventive action (CAPA) report, Market Complain Investigation related activity and its implementation. To review risk assessment and appropriate measures to mitigate the risk and to prevent reoccurrence of risk. Ensuring effectiveness and applicability of the QA system through self-inspection and Quality audit. Improvements / revision in Standard operating procedures as per procedure and their implementation from time to time. To monitor retain samples/logs and physical observation as per standard operating procedure. To monitor stability samples, test frequency and summary results. Monitoring of necessary testing being carried out timely as per specifications and method of analysis and release of certificate of analysis. To monitor maintenance/ repairing of instruments and their annual maintenance contract from external agencies. Co-ordination with public testing labs for timely test report. Getting technical agreement with them, pay visit at time of test to monitor correct method of analysis, whenever necessary. Interdepartmental co-ordination for smooth working to reduce down time in mfg. & packing of various products. To manage for incidents for all testing related chemicals/ apparatus/ standards/ media/ accessory/ parts/ books/ stationary/ dress/ men power requirement, new machine requirement. etc, for timely testing for API/ excipients/ In-process/ finished products/ stability samples etc. Supervision, guidance and inspiration to down the line colleagues for improvement of systems with respect to quality/ data integrity/ efficiency/ correct work procedure etc. To investigate Out of Specification/Out of trend and take appropriate corrective action and preventive action as per standard operating procedure. To prepare risk analysis documents and monitor for probable risks in testing/ reporting, train staff accordingly. Active participation in technology transfer and validation exercise. Evaluation and monitoring of trend data. Monitoring soft data management. To Review and Approved Finish Product (Injection/API), Raw material, Packing material Specification, Standard Operating Procedure, Analytical Work record. To release and approved Raw material / Packing Material in SAP system along with Certificate of analysis (COA). To approved Certificate of analysis (COA) and Release the Semi-finished & Finish product in SAP system. (i.e. I1 and A1) To conduct internal audit / External Audit / self-inspection to ensure compliance to GMP and other regulatory

Job title ADL executive Division phrama Function Analytical method validation Location dombivali Designation ADL executive Job Grade Reporting to (position) ADL Head Direct Reportees (Nos) Company Name Aart industries limited Key Role & Responsibilities 1)Able to performed method validation on GC HS 2)analytical method transfer 3) Able to performed method validation on GCMS 4)method development on GC 5)Handling incident and deviation 6) online review of system,log books 7)Aware of 21 CFR part 11 guidlines ICH and Anvisa Guidlines 8) GC MS and LCMS Linkages within / outside the organisation Internal External Job specification Experience min 9 years Qualification MSc CTC Range as per company based on skill and knowlage Target Company if Any Certifications/Trainings Skills / Competencies Have good knowledge of GC gcms Awareness 21 CFR part 11 knowledge of GMP and GDP handled OOS,OOT incident deviation able to work in shifts. analytical method validation FDS study and photostability Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities 1) To perform the analysis by following cGMP, GLP, ALCO+, and safety compliance 2) To perform the sampling, testing of RM, PM, In-process, Intermediate and Finished product. 3) Participate in Investigation of deviation, Incident, OOS etc. 4) To perform all qualification activities of instrument and equipment in QC Lab. 5) Aware of calibration and operation procedure for instruments ( balance, K.F, GC. UV,refratometer and viscometer etc,) 6) Experience of QC software like Tiamo 3.0, Lab solution, SCM etc. 7) Preparation of documents ( SOP, protocol etc) related to Quality control.

Key Position in Central Team of Motherson Health & Medical to shape, plan and execute Regulatory strategies for Products as part of Organic growth as well as interfacing with Inorganic growth opportunities to assess regulatory risks. Required Candidate profile BE or BTech. or high or equivalent Degree. MBA is added preference. Working Knowledge of Regulatory Resources & Added certifications Ex: RAPS, regulatory trainings and certifications.

JOB DESCRIPTION 1) ARD Scientist (Analytical Research & Development Scientist) Positions Sr Scientist -1 Junior Scientist-2 Job Description: ARD Sr Scientist/Jr Scientist capable in developing and validating analytical methods and Validation including calibration to ensure the quality and stability of pharmaceutical products. Key Responsibilities: Develop and validate analytical methods for drug substances and drug products. Perform analytical testing such as HPLC, GC, and wet analysis. Interpret analytical data to assess product quality, purity, and stability. Implement GLP & GDP practices. Prepare technical reports and documentation for regulatory submissions. Collaborate with the FRD & DQA to support product development. Troubleshoot analytical method issues and recommend improvements. Qualifications: Masters degree or Ph.D. in instrumental analysis, Analytical Chemistry, or related discipline. Expertise in analytical techniques such as HPLC, GC, and spectroscopy. Strong knowledge of regulatory guidelines such as ICH and FDA. Good documentation and report-writing skills. Problem-solving and analytical thinking abilities. Minimum 3(or) More Years for Junior scientist of experience in ARD /Q.C . For Sr Scientist 8 (or) more years of experience is desired 2) FRD Scientist (Formulation Research & Development Scientist) Positions Sr Scientist -1 Junior Scientist-2 Job Description: FRD Sr Scientist/Jr Scientist is responsible for the research and development of pharmaceutical formulations, ensuring the products are safe, stable, and effective for consumption. Key Responsibilities: Design, develop, and optimize formulations for pharmaceutical or nutraceuticals Etc. Implementation of QbD . Conduct experiments to test product stability, and efficacy. Prepare technical documents, including formulation protocols and reports. Collaborate with cross-functional teams such ARD, DQA Etc to ensure compliance. Troubleshoot formulation issues and propose solutions. Qualifications: Masters degree in pharmaceutics or Ph.D. in Pharmaceutics & Equivalence, Minimum 3(or) More Years for Junior scientist of experience in FRD /R&D . For Sr Scientist 8 (or) more years of experience is desired Strong understanding of Good Manufacturing Practices (cGMP). Problem-solving skills and GDP implementation Skills in usage of software for developing of formulation and characterization. Excellent communication skills to present findings and collaborate with teams. Exposure in developing Liquid Orals, Solid Orals, Semi-Solid Orals. Nano formulations will be preferred 3) DQA Team (Development Quality Assurance Sr. Executive) Positions Sr Executive -1 Jr Executive -1 job Description: DQA Sr. Executive should monitor the quality assurance processes during product development, ensuring that all stages comply with quality standards and regulatory requirements and product specification need as per ICH Guidelines. Key Responsibilities: Lead quality assurance activities for product development, including design, testing, and validation stages. Ensure compliance with regulatory guidelines and quality standards (e.g., FDA, EMA, GMP). Develop and implement quality control procedures for new product development. Conduct internal audits and prepare quality assurance reports. Collaborate with R&D, ARD to implement the quality issues. Manage risk assessment processes and ensure continuous improvement in quality systems. Should have knowledge in QbD system for product development. Qualifications: Minimum experience should be 6-8 Years for sr executive and 1 to 3 years for junior executive in DQA (or) Q.A Bachelors or Masters degree in Quality Assurance /Analysis/Pharmaceutics, In-depth knowledge of cGMP, GDP, GLP, ICH and regulatory requirements and implementation. Excellent communication and problem-solving skills.

QC officer Perform chromatographic analyses and tests, including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and Thin-Layer Chromatography (TLC), on raw materials, in-process materials, and finished products. Required Candidate profile Urgent looking for Male candidate who is able to work in rotation shift.

Relevant 6-8 years having Electromechanical Background. Strong experience in creating and managing documentation, such as Good Documentation Practices (GDP), in regulated industries like medical devices, pharmaceuticals, and aerospace. Proficient in statistical tools such as Minitab, with experience in techniques like ANOVA, t-tests (1t, 2t), Gage R&R, DOE (Design of Experiments), Monte Carlo simulations, and understanding statistical concepts like resolution. Solid understanding of translating Design Master Records (DMR) into production processes, with knowledge of both R&D and manufacturing activities (similar to roles like an industrialization engineer at Philips). Proven ability to communicate clearly and collaborate with global stakeholders, and effectively manage multiple manufacturing activities across teams. Experience performing and guiding product validation tests (such as TMV, IQ, OQ, and PQ) directly on the shop floor. Ideally, a background in verification or validation within regulated industries.

Looking for candidate with 3-4 years of experience in Quality Assurance in Edible oil.

Client Location: Tower B, 16th Floor, Prestige Shantiniketan, Bangalore North, Bangalore, 560048 Role: Tester - Skill Set 3 Senior Client Domain: Healthcare, Medical Devices manufacturing Business Unit: Kidney Care - Kidney Care Multi Division (158-105) Job Description: Essential Duties and Responsibilities: Contributes through demonstrated hands-on participation in Leading Engineering Change controls & Testing activities. Exposure to GDP and GMP is must. Hands on Experience in handling Mechanical Equipment like UTM, Leak Tester, Torquer Tester and other instrument and Equipment would be added advantage Ability to write testing protocols independently with minimum guidance. Hands on experience in Creo or SolidWorks is must. Responsible for Design and Development of fixture per V&V needs by preparing drawing and working closely with external vendors. Responsible & Accountable for project deliverables. Lead all DHF tasks & Risk management tasks Hands on. Work with Cross Functional Teams Globally ensure completion of Cross functional tasks. Experience in Handling Plastic components, Design of Connectors is preferred. Exposure to Regulatory Standards and Manufacturing process and procedure for Medical Devices. Exposure to RF welding, Solvent bonding process would be an added benefit. Exposure to statistical tools like Minitab and Six sigma methodology for results analysis would be an added advantage. Ability to Plan DoE to resolve any issues to technical discussion and support and product install based. Ability to conduct verification and validation tests to support changes as per QMS process. Ability to do project planning for Leading the installed base tasks. Ability to resolve to field issue - Perform NCR/CAPA. Responsible for completion of MDR activities related to assigned families. Responsible for executing all assigned test with minimal dependency on owners by considering testing timelines, providing frequent updating of test results to owners, and ownership in preparing final report by routing, review signoff and releases. Qualification: BE in Mechanical Engineering with 7 to 10 years of experience in Medical and Aerospace Domain.

1.Responsible for batch record issuance. 2 Responsible for issuance of change control 3.Resposible for implementation of ISO & Quality Management System 4. Responsible for calibration & validation of Equipements & Instruments 5. Responsible for inprocess Quality Checks 6.Resposible to implement CGMP 7. Responsible to monitor product activity 8. Responsible for issuance & retrival of control document 9. Resposible for dispatch verification 10. resposible to prepare process validation proyocal & record

Role & responsibilities Responsible to receive, register and analyze batch samples and stability samples. Responsible to prepare reagents, buffers and test solutions as and when required. Responsible to operate, calibrate/ verify/ qualify HPLC, UPLC instruments. Responsible to execute the Analytical Method validations/verifications/Transfers Responsible to prepare SOPs, STPs, Protocols and other GMP documents Responsible to interpret and record the data / results accurately and contemporaneously. Responsible to report to superior any abnormalities found during routine activities Responsible to follow Hygiene, Safety, SOPs, GLP, GMP and GDP. Preferred candidate profile Adequate testing knowledge on Biologics/Monoclonal Antibodies Capillary Electrophoresis : CESDS-R, CESDS-NR HPLC : RP, SEC, Glycan, CEX, Ion exchange chromatography and Polysorbate 20 Maurice : charge variants by iCEF UPLC : Peptide mapping. Qualification and Experience : MSc Biotechnology/Biochemistry/Microbiology with 03-07 Years experience of Biosimilars/Biologics QC.

JOB DESCRIPTION: Perform calibration of analytical instruments and online documentation as per GDP requirements. Work as per Good Laboratory Practices. Maintaining log books, Column usage cards and calibration records . Report preparation.

B.Sc. / M.Sc. with 3 to 4 years of experience in pharmaceutical industry. Experience of CAPA, change control, QMS, Documentation, SOP Preparation, IPQA, BMR issuance and review, Equipment qualification, GMP/GDP documents, etc. Required Candidate profile To ensure Q. A. activities are carried out as per set procedures and ensure to record in respective documents. Preparation and review of equipment and utility qualifications documents. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top management level professionals according to clients specific needs. We are BEST-FIT Recruitment Riders do exactly what our name tells. To know more about us please visit our website: www.bestfitrecruitment.co.in We would like to inform you that presently we have professional career opportunity matching to your profile with one of our esteemed client. Please see the following position summary: Client Name: USA based Pharma manufacturer Position : Manager - Logistic Management / SCM (International) Location: Vadodara Job Profile: Manage end to end international logistic activates for global movements of APIs & Advanced Intermediates. Acts as a first line resource to manage the interface between functions pertaining to supply, transportation, logistics, and traceability issues. To develop systems and processes so that the Logistics dept. works closely with Stake holders. Arrange transportation and logistics for the delivery of goods and materials to project sites, partner organizations, and beneficiaries. Plans, executes, & tracks international shipments by maintaining close partnerships with Distribution & Carrier Contract Service Providers. Coordinate with shipping companies, freight forwarders, and customs agents to manage imports, exports, and cross-border logistics. Track shipments and ensure on-time delivery while minimizing costs and delays. Select carriers for transportation and negotiate rates and contracts with carriers. Supervise, coach and train logistic workforce. Excellent communication and interpersonal skills, with the ability to work effectively with diverse teams and stakeholders. Co-ordinate with internal Purchase department, Logistic department for timely supply. Maintain and update the customer database timely. Knowledge of relevant regulations and compliance requirements in logistics and supply chain management. Identify areas for improvement and implement corrective actions to enhance logistics efficiency and effectiveness. Adhere to the companys guidelines as set out in the standard operating procedures. To conduct Financial Analysis on the Logistics Costs. Resolve any arising problems and complaints. To work across all functions within the organisation to synergies and with a purpose of meeting the organisational goals. Desired Profile: Any Graduate + PGDSCM / MBA (SCM / Logistic) with 10 to 15 years experience with well-known Pharmaceuticals preferably from a multi-national organization. Additional Certifications: Logistic / Dispatches would be added advantages. Proven working experience in Logistic Management especially in International. Knowledge of relevant regulations and compliance requirements in logistics and supply chain management Experience in managing Carriers and Customs Agents in USA, as well as knowledge of USFDA regulations in regard to import and export of Pharmaceutical goods. Good knowledge of end to end logistics operations. Sound knowledge of Customs procedures (Pre Export & Post Export). Adaptability and Flexibility in logistics operations. Excellent communication and interpersonal skills, with the ability to work effectively with diverse teams and stakeholders. Strong critical thinking and negotiation skills. Ability to work independently and with internal stakeholders at all levels of the organization. Fluency in English, written and oral. Language proficiency: English, Hindi, Gujarati (must). Recruiter Details: BEST - FIT Recruitment Riders G-7, Amrit Complex, Opp: Mahavir Jain Vidhyalaya & Jain Derasar, R.V. Desai Road, Near Goyagate Circle, Vadodara-390001, Gujarat, India E-Mail: career@bfrr.in Website: www.bestfitrecruitment.co.in

Responsibilities - HPLC Analysis of FG, RM, Stability samples etc. - Ensure GLP, GMP & GDP compliance. - Ensure the preparedness for Audits. - To perform calibration of QC instruments. - To perform QMS activities. - Knowledge of QC instruments. - Adhere to cGMP, GLP, and GDP practices. Note- Male candidates are preferred due to working in shifts.

implementation of QMS, Quality operations , Management of Product Returns, Handling, Storage of medical products, NC/CAPA at DC,Execute the activities related to QMS elements like Document Control, Change Control, Escalations,