Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.
Role & responsibilities Use of HPLC/GC/UV/Dissolution apparatus. Integration for Assay and RS. Method development and force degradation study for FP and API. Preparation of method development protocol. Dissolution development and impurity profiling. Force degradation study for FP and API. Pharmacopeia method interpretation, Literature/references search. Listing the requirements for method development. Review and interpretation of development trial data. Preparation and review of method development protocol and report. Descriptive method right up.
Role & responsibilities Expertise in OSD, Liquid, Injectable, Ophthalmic & External preparations for ROW, Domestic and Regulated Markets Automation of products, CMO/CDMO packaging development and regulatory documentation Review and approval of new/revised artworks Preparation of MPR/STPs and SOPs Preferred candidate profile Knowledge of solid oral, liquid, injectable, or topical dosage forms.
Role & responsibilities Manufacturing area:- Line clearance before start of batch processing and after cleaning. In-process checks during manufacturing stages Verification of machines settings, process parameters and yield reconciliatoin Sampling of in-process materials for testing. Monitoring of environmental conditions and compliance during production Verification of online entries in BMR Packing area: Line clearance before start of packing and after product/pack change over. Monitoring batch coding, overprinting, labeling, and packaging operations Performaning in-process checks - correct packing components, label reconciliation, and proper sealing. Monitoring controlled area discipline, gowning and hygiene compliance Accuracy in documentation and compliances . Preferred :- Strong observation and documentation skills. Good understanding of pharma documentation practices.
Role & responsibilities Adequate knowledge of respective guidelines. i.e. ICH, USP,WHO, etc. Stability sample analysis by HPLC/GC/UV/Dissolution apparatus. Preparation of stability testing worksheets. Sample charge and withdrawal as per stability condition. Management of stability samples and stability chambers and maintain the schedule. Preparation of stability trend records and summarize the results Review the stability sample testing data. Review the stability analysis worksheet. Review the stability protocols, samples and stability chambers log records. Review of OOS/OOT and co-ordinate with respective concerns.
Role & responsibilities Identify and acquire new clients for domestic contract manufacturing /loan license business. Maintain and strengthen relationships with existing pharma partners. Negotiate product costing, MOQ, payment terms and supply schedules. Strong understanding of pharma formulations and contract manufacturing processes. Proven network with pharma marketing/PCD/B2B companies. Commercial acumen in pricing, costing and profitability management.
Role & responsibilities Overall Facility Management such as housekeeping, pest control, first aid, Canteen etc.. Monitor hygiene standards across production and office areas. Maintain cost control and documentation for all administrative functions. Assist in audits, compliances and facility improvements. Manage employee facilities and general welfare services. Preferred candidate profile Strong interpersonal, proactive, organised and responsible individual.
Exciting Opportunity at Lincoln Pharmaceuticals Limited , We're thrilled to announce 1 opening in our HR Department !!! Role : HR Officer/ Sr. Officer Location: Ahmedabad Key Responsibilities: Handle the end-to-end recruitment process, including sourcing, screening, interviewing, coordinating interviews, and managing offers. Develop and implement effective recruitment strategies to attract top talent in the pharmaceutical industry. Work closely with hiring managers to understand workforce needs and define job requirements. Utilize multiple sourcing channels such as job portals, social media, employee referrals, LinkedIn, and campus hiring. Maintain and update the applicant tracking system and recruitment databases. Build a strong talent pipeline for current and future hiring needs. Ensure compliance with company policies and relevant labor laws during hiring. Requirements: Bachelors degree in Human Resources, Business Administration, or a related field (MBA preferred). Minimum 1 years of proven experience in recruitment, preferably in the HR industry. Strong knowledge of pharma job roles and functions across departments. Excellent communication, interpersonal, and negotiation skills. Immediate joiners preferred Share your CV on ho.recruitment@LincolnPharma.com or on 99981 72682.
Role & responsibilities PACKING (OSD) : Assisting in packing area and production department Dispensing for secondary packing material Documentation of packing area Log Records and B.P.R. and B.M.R Supervision of Packing area Reviews and final reconciliation of BPR & BMR Online Documentation in Process of Packing COMPRESSION /COATING / CAPSULE : Execution and planning of compression / Coating / Capsule activity Troubleshooting of compression machine / Coating machine / Capsule filling Recording of BMR, daily document, cleaning record, issuance of issuance of change part OINTMENT : Supervise and coordinate all aspects of the ointment production process to meet daily, weekly, and monthly targets. Allocate manpower, schedule staff, and guide operators Preferred candidate profile Exposure of audits (EU - GMP/ WHO / ROW ) Willing to work in shifts. Ready to take pressures. Passion to learn. Maintain the cleaniliness of area. Aware about the concept of GMP/GDP/Data integrity. Handling manpower
Role & responsibilities Experience in managing Housekeeping staff. Good Documentation Practices. Preferred candidate profile Preferably within Ahmedabad / nearby areas.
Role & responsibilities Should be able to take responsibilities assigned. Maintain proper documentation of batch records, raw material usage, and production logs. Oversee production activities as per cGMP standards. Preferred candidate profile Willing to work in shifts. Ready to learn and grow Time management and ability to work under deadlines Candidates from Ahmedabad / near by preferred.
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