28 Coa Jobs

1. To prepare technical documents (Specification, MSDS, declarations, etc) for various products. 2. Will be a custodian of documents shared to customer. 3. To attend customer complaints and if necessary coordinate with factory QA team for addressing the issues. 4. To adhere to strict timeline to share customer related documents. 5. Master degree in related field in science 6. Should have prior experience in handling technical documents in botanical industries. 7. Should have basic knowledge about various medicinal plants and their contents 8. Should be a good team player

Dossier Preparation. Interact with Marketing, Quality Control, Product Development, R&D, & manufacturing units to collect necessary documents. MSDS of both Technical & formulation products. Discussions with regulatory team to improve knowledge. Required Candidate profile Must have exp in international regulatory affairs.

Job Title: Quality Control Executive Ayurveda Products Department: Quality Control (QC) Location: Kundli Job Summary: We are seeking a detail-oriented and experienced Quality Control Executive to ensure the quality, safety, and compliance of Ayurvedic products. The QC Officer will be responsible for implementing and maintaining testing protocols for raw materials, in-process samples, and finished products according to GMP and regulatory standards applicable to Ayurveda and herbal formulations. Key Responsibilities: Conduct routine quality checks and testing of raw materials, packaging materials, in-process samples , and finished Ayurvedic products . Ensure compliance with AYUSH regulations , GMP , and ISO standards where applicable. Maintain and calibrate lab instruments such as HPTLC, UV-Vis Spectrophotometer, pH meters, etc. Prepare and maintain Standard Operating Procedures (SOPs) , test reports , COAs , and specifications for materials and products. Conduct microbiological testing and stability studies as required. Collaborate with the R&D, production , and QA departments for troubleshooting and quality-related investigations. Handle non-conformance reports (NCRs) and support in CAPA implementation . Review batch manufacturing records (BMRs) and ensure quality documentation is in place. Support in regulatory audits (AYUSH, FSSAI, WHO-GMP, etc.) and third-party inspections. Requirements: Education: B.Sc. / M.Sc. in Chemistry, Microbiology, Biotechnology, or B.Pharm / M.Pharm (Ayurveda or Pharmaceutics preferred). Experience: 2–5 years of experience in Quality Control in an Ayurvedic / herbal / pharmaceutical company . Skills: Knowledge of Herbal Pharmacopoeia , Ayurvedic raw materials, and formulations. Familiarity with regulatory frameworks like AYUSH , WHO-GMP , and FSSAI . Good analytical, problem-solving, and documentation skills. Proficiency in laboratory practices and equipment handling. Preferred Qualifications: Experience with HPTLC , TLC , moisture analysis , ash value , and extractive value testing. Knowledge of modern analytical techniques used in herbal product testing. Basic understanding of Ayurveda / Unani / herbal systems . es Preferred candidate profile Contact us on nancy@atiyahealthcare.com OR contact on whatsapp 9773743345

Dossier Preparation. Interact with Marketing, Quality Control, Product Development, R&D, & manufacturing units to collect necessary documents. MSDS of both Technical & formulation products. Discussions with regulatory team to improve knowledge. Required Candidate profile Must have exp in international regulatory affairs.

Position: Documentation Executive Analytical R & D Looking for candidates with 3+yrs of experience as Documentation Executive Total Experience: 3-6yrs Qualification: M Sc Location: Bangalore (Peenya 2nd Stage). Roles & Responsibilities Should have knowledge and exposure of SAP Software. Should be well versed with documentation procedures, preparation and review of Certificate of Analysis and specifications. Preparation and uploading of new finished product specifications, revision of existing finished product specifications, release of CoAs for finished products received from the units. Preparation of MSDS, work order requests, work order completion, and CoAs for samples tested for both inter-departmental and intra-departmental use. Should have good communication skills.

Studying Legal Documents and collating info in a variety of formats. Ensuring compliance with regulations set by the Cosmetics & Perfumes Regulatory Agency as country wise Keeping up to date with changes in regulatory legislation and guidelines Required Candidate profile Well versed with US FDA, EU regulatory requirements Be well versed in the preparation of MSDS, COA, PIF and CPNP files Knowledge on Indian Drug & Cosmetic mfg Act especially on Schedule S Stds & GMP.

Reporting to Sr. Director - Regulatory Affairs Experience required: 5-8 Years Education: B. Pharm / M. Pharm Department: Regulatory Affairs Key Responsibilities: Prepare the status of all documents related to submission. Compile and review Regulatory submission documents required in line with the relevant guidelines. Coordinate with all stakeholders of the manufacturing plant for the collection of documents. Evaluation of change control: evaluate all post-approval changes. Review of specifications (API, Intermediate, FP, and Shelf life) executed BMRs, BPRs, COA, Method transfer report, Method verification, Analytical chromatograms intended for regulated or non-regulated market submission. General Review of plant Site Master File, layouts, and valid GMP Compliance Certificate for its adequacy to support regulatory submission. Effectively implement post-approval commitment. Preferred candidate profile Review of CMC (Chemistry, Manufacturing, and Controls) Documents Self-motivated, detail-oriented, and highly organized professional Proven ability to collaborate and communicate effectively with diverse teams Proficient in Microsoft Word, Excel, and PowerPoint Fluent in English, with strong skills in speaking, comprehension, reading, and writing. Strong technical expertise in reviewing manufacturing site documentation.

About Client Hiring for One of the topmost MNC!! Job Description Job Title: MES Camstar Developer Qualification : Any Graduate or Above Relevant Experience : 3 to 15 Years ROLES AND RESPONSIBILITIES Act as a Solution Architect for Camstar/Opcenter MES projects Lead and manage the design and development of CIO/MIO Maps and related workflows Gather and translate user requirements into functional specifications Responsible for the end-to-end implementation of MES solutions Coordinate with cross-functional teams and ensure timely delivery Manage and distribute work effectively across the development team Ensure adherence to regulatory and quality standards relevant to the industry Technical/Functional Skills Strong hands-on experience with Camstar Designer and Camstar Portal Development Expertise in COA/CIO/MIO interface connectivity Experience in large-scale, global MES implementations with full project lifecycle ownership Proven experience in the implementation of Manufacturing Execution Systems (MES), especially Camstar/Siemens OpsCenter as a COTS solution Hands-on experience with Camstar Upgrade and Factory Model Strong domain knowledge in Medical Devices and/or Pharma Manufacturing Proficient in integrating Camstar MES with external systems like ERP, LIMS, Equipment, HMI Good understanding of computer systems validation (CSV) and manufacturing validation processes Strong SQL skills Exposure to Azure Kubernetes or similar cloud-native technologies is a plusGeneric Managerial Skills Strong communication and interpersonal skills Adaptable, quick learner, and results-driven Demonstrated leadership capabilities, with experience leading project teams Ability to manage multiple priorities in a fast-paced environment Excellent team collaboration, with a focus on motivation and team development Skilled in facilitating clear and effective communication across stakeholders; Location : Pune , Hyderabad , Chennai , Bangalore CTC Range : 20 LPA TO 40PA Notice period : ANY Shift Timing : N/A Mode of Interview : VIRTUAL Mode of Work : WORK FROM OFFICE Preethi R Senior Staffing Analyst Black and White Business solutions PVT Ltd Bangalore, Karnataka, INDIA. vardhani@blackwhite.in I www.blackwhite.in

About Client Hiring for One of the topmost MNC!! Job Description Job Title: MES Camstar Developer Qualification : Any Graduate or Above Relevant Experience : 3 to 15 Years ROLES AND RESPONSIBILITIES Act as a Solution Architect for Camstar/Opcenter MES projects Lead and manage the design and development of CIO/MIO Maps and related workflows Gather and translate user requirements into functional specifications Responsible for the end-to-end implementation of MES solutions Coordinate with cross-functional teams and ensure timely delivery Manage and distribute work effectively across the development team Ensure adherence to regulatory and quality standards relevant to the industry Technical/Functional Skills Strong hands-on experience with Camstar Designer and Camstar Portal Development Expertise in COA/CIO/MIO interface connectivity Experience in large-scale, global MES implementations with full project lifecycle ownership Proven experience in the implementation of Manufacturing Execution Systems (MES), especially Camstar/Siemens OpsCenter as a COTS solution Hands-on experience with Camstar Upgrade and Factory Model Strong domain knowledge in Medical Devices and/or Pharma Manufacturing Proficient in integrating Camstar MES with external systems like ERP, LIMS, Equipment, HMI Good understanding of computer systems validation (CSV) and manufacturing validation processes Strong SQL skills Exposure to Azure Kubernetes or similar cloud-native technologies is a plusGeneric Managerial Skills Strong communication and interpersonal skills Adaptable, quick learner, and results-driven Demonstrated leadership capabilities, with experience leading project teams Ability to manage multiple priorities in a fast-paced environment Excellent team collaboration, with a focus on motivation and team development Skilled in facilitating clear and effective communication across stakeholders; Location : Pune , Hyderabad , Chennai , Bangalore CTC Range : 20 LPA TO 40PA Notice period : ANY Shift Timing : N/A Mode of Interview : VIRTUAL Mode of Work : WORK FROM OFFICE Vardhani IT Staffing Analyst Black and White Business solutions PVT Ltd Bangalore, Karnataka, INDIA. 8686127477 I vardhani@blackwhite.in I www.blackwhite.in

Preparation of Technical documents like below: COA/ Certificate of Analysis Specifications/ TDS Method of Analysis Stability Data DMF/ Drug Master File Declarations Preparation of Vendor Questionnaire Customer response for technical queries

Preparation & Review of dossier in CTD, ACTD, ETCD format Preparation of dossiers of stability Data, Analytical method validation Preparing the SPC/SMPC as per country guidelines Preparation and Reviewing of documents COA as per the country guideline

Role & responsibilities : Coordinating with Production, ware house and quality assurance uninterrupted release of Raw materials, Water samples and In-process samples. Analysis of In-process, Raw materials and water samples (Chemical analysis) Handling of pH, Conductivity meter, and TOC Analyser (Make Shimadzu). Ensure compliance of various quality measures such as GLP by maintenance of appropriate requisite documentation/ records Ensure compliance of various quality measures such as GLP by maintenance of appropriate requisite documentation/ records Good communication skills Preparation and review of COAs Qualification: MSC-Analytical Chemistry/ Organic Chemistry/ B Pharmacy/ M Pharmacy/ Microbiology

AX , 3+ End-to-End implementation of Dynamics 365 Finance & Operations, Dynamics AX 2012 R3,Core finance domain knowledge, knowledge in General ledger, AR, AP, Fixed asset, Budget, Cash and Bank management, Required Candidate profile Notice Period: 0-30 days Education: BE, B.Tech, ME, M.Tech

Role & responsibilities Preferred candidate profile Perks and benefits

Head API Intermediates Procurement : We are looking for an expert API Intermediates Purchaser with a strong background in sourcing from China. The ideal candidate must have deep knowledge of general API intermediates (e.g., 6-APA for Amoxicillin) and oversee strategic procurement, cost negotiations, and supplier management Key Responsibilities: - Procure API intermediates used in general API manufacturing (penicillins, cephalosporins, macrolides, etc.) - Strong network in China as well with expertise in import regulations & pricing trends - Analyze COAs, ensure quality compliance, and manage purchase orders - Negotiate best rates & build long-term supplier relationships - Monitor market trends, regulatory updates, and supply chain risks Requirements: - 10+ years in API intermediates procurement (China sourcing expertise is a must) - In-depth knowledge of intermediates for general APIs (e.g., 6-APA, 7-ACA, etc.) - Excellent negotiation & vendor management skills - Experience in bulk purchasing & import/export regulations . Perks: Competitive salary, performance incentives, career growth, and health benefits. Ready to lead API intermediates procurement? Apply now!

Interview for Female for QA Department for Chemical Company in Dahej on 4 & 5 April Qualification: BSC / MSC Chemistry Experience: 3 to 7 Years CTC: Up to 6 LPA Only Female Share with your Female Friends Free Jobs, No Placement Charges Required Candidate profile Send CV on sdpbharuch@gmail.com with Subject: QA Female Dahej Join WhatsApp Group: https://chat.whatsapp.com/LelLOsEoGgmIaK6EBrWZWN Follow Us: https://whatsapp.com/channel/0029VaDwTZoHgZWddec9BL0y

Required MSC Chemistry with 2 to 4 years experience in organic chemistry in Chemical industry To carry out R&D expertise in lab & Pilot plant, To oversee job work. Should have experience in Gas Chromatography (GC) Required Candidate profile Literature work, regulatory work ( reach, DSIR etc.) Technical data management Maintening SDS,TDS folder, Luba & Mining data Making CoA/Analytical reports

1. COA/ Certificate of Analysis 2. MSDS 3. Specifications/ TDS 4. Method of Analysis 5. Stability Data 6. DMF/ Drug Master File 7. Declarations B. Preparation of Vendor Questionnaire Required Candidate profile C. Customer response for technical queries D. Must have knowledge of Pharmacopoeias, ICH guidelines Intrested Candidate Can connect on 91-9724346949 / 9327657730

Role & responsibilities Preferred candidate profile 1. Responsible for the Change control Handling through Track wise related to Spec & STP & CAPA 2. Prepare the Specification & Standard testing procedure of API Site. 3. Review of Method of analysis (MOA), Specification, STP of RM, IM, PM, INP, API & Cleaning generated by R&D Analytical. 4. Review of Standard qualification COA. 5. Review of Method comparison & MOA with Pre-validation data 6. Review of Validation Protocol & validation Report with respect to analytical data and Journal. 7. Review of R&D batches Stability data. 8. Issuance, login and closing of Incidence and change control of DQA/R&D-synthesis/R&D-Analytical. 9. Issuance of format, Logbooks, BMR and uncontrolled copy of MOA and/or Spec & STP. 10. Document and data control i.e. Receiving, Issuance/Distribution, Archival, Control, Storage and destruction of documents. 11. Assigning analytical method validation protocol and Report Numbering. 12. Responsible for sample management activity (i.e. Receiving, Issuance and Discard)

Urgently looking for IMPORT Documentation Specialist JR Officer / Officer / Senior Officer Role & responsibilities - JR Officer / Officer Responsible for handling Imports & Shipping Operations from Global supplier vendors Pre & Post Shipping Documents Processing Shipping documents /AWB, COA, Insurance ,BL, BOE, EPCG, GST, HSS. Ensuring Customs & DGFT Compliance to all legal and Regulatory Requirements (Relevant to Shipping Logistics, Imports) . Global Supplier Management. Knowledge about Tally ERP PO Creations in ERP / Purchase contract agreements as per company norms Managing Customs clearance, CHAs Job allocation, Freight Forwarders and Inland Transports & Delivery processing to factories Commercial Invoice Accounting (Suppliers, Clearance & forwarding cost, Transport & CFS) Liaison with Global Suppliers for Mitigation Quality Issues & Inspections Responsible for Bill of Entry & Checklist. Knowledge in EXIM (Manufacturing Industry), Customs Tariff & DGFT policies Preferred candidate profile Relevant Experience in Metal or Manufacturing Industry will be an added advantage JR Officer / Officer: 02 to 04 years of relevant experience Senior Officer / AM / DM / Manager: 05 to 12 years of relevant experience Gender: Male or Female Qualification: Any UG / PG Perks and benefits Paid Leave, Leave Encashment, Bonus and Medical Insurance Only relevant experience candidates, please share your resume to following email address hr@sabharismelters.com or through What's App 7092549951 / 8925921300 and Others kindly ignore. Relevant experience candidate can directly come for face-to-face interview between 11:30am to 04:30pm at below mentioned venue between Monday to Saturday. Venue: No.180, Capital Towers, 01st Floor, M.G.R Salai, Kodambakkam High Road, Nungambakkam, Chennai - 600034. Landmark: Opposite to Hotel Palmgrove

Required MSC Chemistry with 2 to 4 years experience in organic chemistry in Chemical industry To carry out R&D expertise in lab & Pilot plant, To oversee job work. Required Candidate profile Literature work, regulatory work ( reach, DSIR etc.) Technical data management Maintening SDS,TDS folder, Luba & Mining data Making CoA/Analytical reports

Position: QUALITY ASSURANCE (QA) MANAGER Description: The ideal candidate will be responsible for overseeing the quality and safety of our food products, ensuring they meet all regulatory and company standards. This role involves developing and implementing quality assurance policies, conducting regular inspections and audits such as BRCG 9 and FSSC 22000. The QA Manager will work closely with production, procurement, and QC teams to ensure that our products are safe, consistent, and of the highest quality. Verication of HACCP, validation, test methods, updating of SOP's. Preparing customer specications, COA, and other vendor related documentation. Thorough knowledge of Export documentation knowledge related to quality assurance along with CAPA & Root cause analysis. Coordinating with external laboratory testing of FG, PM, Water As per FSSAI and Organic sampling as per APEDA. This position requires a proactive approach to problem-solving and a commitment to continuous improvement. Deliver training programs for sta on quality standards, food safety and hygiene. Stay updated on industry trends and regulatory changes. Develop and implement corrective action plans. Experience: 5-8 years Education Qualification: B-tech / M-Tech Food technology / Msc Biochemistry, Biotechnology, Microbiology, Msc Food Science & Nutrition Industry Type: Agriculture/Biochemistry/Technology /Food technology (Agri-tech) Role Type: Individual Contributor Employment Type: Full Time, Permanent

Hello Candidate, Greetings of the day Hungry Bird !! We are currently hiring for Quality Shift In charge for one of our client. Location : Hyderabad Job Summary: The Quality Shift In charge is responsible for ensuring that all products meet the company's quality standards. This includes inspecting products, identifying and resolving quality problems, and documenting quality control activities. The Quality Shift In charge also provides training to team members on quality and food safety. Responsibilities:- Should maintain the company policy of personal hygiene, GMP and safety Requirements along with safeguarding the company assets as their primary responsibility. Preparation of line release documentation. Update and review and Client HACCP document. Co-ordinate with Client Block related external lab agency for timely collection of samples related to air monitoring, water, raw material and finished goods, verification of above testing reports, filing, and Invoice submission to accounts department. Ensure compliance with clients block RM, PM; FG QMS. Review and approve Client block inhouse testing report and sign document in absence of HOD. Prepare and execute the Client trial and related activity. Update Client block KPI sheet and OTUD calculation. Timely implementation of products traceability and Mock recall activities as per schedule. Timely Investigation of Client block related customer complaint, OTR & Report preparation. Timely PMP - revisions, results tracking & Follow-up of sampling. Participate in Client operation review meeting with concerned team members. Verify and ensure the compliance to customer requirements of GMP, GHK, Company Quality and Food Safety Policy. Conducting process and Internal audits providing timely communication to Inter & Intra departmental as per schedule. Participate and act as coordinator in Client sensory session in absence of lab in charge. Preparation of Client zoning plan & Pest control layout. Timely updating of Client Block related price circular & Shelf-life display sheet and take sign off from other departments. Participate in proficiency and result reporting to Client. Provide updated Client specification, testing procedure to RM/PM Chemist. Follow up of KQ plan for newly added SKU's and change of existing SKU's with clients co-man quality. Method monitoring and method verification. Operate the lab in line with the Clients GLP requirements. Authorities:- To Provide training to team members on quality and food safety and customer requirements sensory screening documentation - RM, attribute, basic & advanced. To release the SFG, PM & FG in SAP transactions. To verify and sign the testing report, LPR and act as Deputy to HOD in absence of HOD. To hold the non-complied or OOS product and stop the process and packing line in case of any deviations. To participate in all types of Trial and Sensory sessions and report generation, communication with concerned. To file all LPR, calibration, testing report, customer specification and storage in record and disposal post completion of retention period. To raise the indents as per requirements in the department and coordinate with accounts department for PO preparation. Interested candidates can share their CV to renu@hungrybird.in / 8885825360 priya@hungrybird.in / 8008832123 hr@hungrybird.in / 9701432176 Please furnish the below-mentioned details that would help us expedite the process. PLEASE MENTION THE RELEVANT POSITION IN THE SUBJECT LINE OF THE EMAIL. Example: KRISHNA, HR MANAGER, 7 YEARS, 20 DAYS NOTICE Name: Position applying for: Total experience: Notice period: Current Salary: Expected Salary: Thanks and Regards renu@hungrybird.in / 8885825360 priya@hungrybird.in / 8008832123 hr@hungrybird.in / 9701432176

Hello Candidate, Greetings of the day from Hungry Bird!! We are currently hiring for Lab Incharge for our client. Location : Hyderabad. Job Summary: The Lab Incharge is responsible for overseeing the daily operations of the laboratory, ensuring compliance with safety and quality standards, and maintaining accurate records. This role involves conducting tests, managing samples, calibrating equipment, and training lab personnel. Responsibilities: Should maintain the company policy of personal hygiene, GMP and safety Requirements along with safeguarding the company assets as their primary responsibility. Conducting the checks for Clients block incoming checks for SFG / PM, FG as per customer specification. Clients block sample collection, identification, analysis and documentation. Sending courier samples to external testing lab and submission of invoice to accounts department. Train the lab helper in case of any requirements and change in existing practices. Verify and ensure the compliance in day-to-day lab operations. Carry out internal calibration of lab equipment's. Operate the lab in line with the GLP requirements. Communicate to HOD in case of any abnormality, deviations observed. Maintain the overall housekeeping of Lab, Timely disposal of samples. Monitor the retention sample and timely disposal in consultation with HOD. Track the courier samples sent. Participate in Clients customer complaint investigation. Authorities: To communicate with vendor with respect to online rejection in incoming material. To hold the incoming material with deviation in consultation with HOD. To raise the indents for lab as per requirements and coordinate with accounts department for PO preparation To maintain only update version of specification, artwork, shade card. To remove the obsolete copies of documents and discard as per SOP. To share the in-house testing report and COA with customer Prepare the COA for in house testing samples. Interested candidates can share their CV to renu@hungrybird.in / 8885825360 priya@hungrybird.in / 8008832123 hr@hungrybird.in / 9701432176 Please furnish the below-mentioned details that would help us expedite the process. PLEASE MENTION THE RELEVANT POSITION IN THE SUBJECT LINE OF THE EMAIL. Example: KRISHNA, HR MANAGER, 7 YEARS, 20 DAYS NOTICE Name: Position applying for: Total experience: Notice period: Current Salary: Expected Salary: Thanks and Regards renu@hungrybird.in / 8885825360 priya@hungrybird.in / 8008832123 hr@hungrybird.in / 9701432176

Responsible perform/Report the analysis of Water and pure steam (Condensate) samples. Responsible for preparation of Standard operating procedures, Standard test procedures, specifications ,SOP, STP, Specification, ATDS CoA of the RM, PM, Consumable Required Candidate profile change control /deviation / OOS / OOT / OOC/CAPA. Analytical method transfer/Stability Protocols Report the analysis of Finished Product, In- IP, SFG, FP. Perform the analysis as or when required