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4.0 - 9.0 years

4 - 9 Lacs

Hyderabad

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Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. We have opening for Formulation R&D Department - oral solution exp or Injectable Experience : 2-10 Yrs Job Location: Pashamylaram - Patancheruv Job Description: Candidate must have knowledge-Literature Search, Product Development,Scale-up Batches, Characterization, Prototype Development, , Exhibit Batches, DOE Experiments , PDR Preparation & Development related documentation. Experience in US ,EU Markets .Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current C T C : Exp C T C : Notice Period: Current Designation:

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4.0 - 9.0 years

4 - 9 Lacs

Hyderabad

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Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. We have opening for Formulation R&D Department - oral solution exp or Injectable Experience : 2-7 Yrs Job Location: Pashamylaram - Patancheruv-Sangareddy Dist. Job Description: Candidate must have knowledge-Literature Search, Product Development,Scale-up Batches, Characterization, Prototype Development, , Exhibit Batches, DOE Experiments , PDR Preparation & Development related documentation. Experience in US ,EU Markets .Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current C T C : Exp C T C : Notice Period: Current Designation:

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3.0 - 8.0 years

3 - 8 Lacs

Hyderabad

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Dear Respect Applicants. Greeting from Biophore India pharmaceutical Pvt Ltd. (oral solution exp) or Inject able We have opening for Formulation R&D Department. 1) Candidate must have knowledge Prototype & Product Development. 2) Must have Literature Search. 3) Scale-up Batches, Exhibit Batches, DOE Experiments. 4) PDR Preparation & Development related documentation. 5) Experience in US ,EU Markets. 6) Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. 7) Good Communication Skills. Role & responsibilities Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current CTC: Exp CTC: Notice Period: Current Designation:

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8.0 - 12.0 years

9 - 12 Lacs

Thane, Mumbai (All Areas)

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Role & responsibilities To lead the OSD department team and ensure manufacturing process development and Optimization as per the regulatory requirements & technology transfer of the projects in co-ordination with Production and planning department for regulatory & ROW products. Accountabilities and mandatory requirements: Ensure composition and manufacturing process development of new as well as established products and ability to improvise if needed. Ensure manufacturing process/new process within Budget for maximizing efficiencies of Formulation Department Lab. Guide group for day-to-day activities and informing Formulation Development Department (FRD) colleagues for the schedule and timelines for the product development as well as technology transfer of Exhibit, Validation or commercial batches. Ensure group co-ordinate with other functions including Purchase, Production for the status of availability of Raw Materials, Packaging Materials required for development batches/ exhibit batches/ Validation batches at site. Ensure development and stability data generation of the new as well as trouble shooting products as per the regulatory or ROW market requirements. Guide to the for encounter the trouble shooting of legacy products and to provide the Technology transfer documents to resolve or to overcome issues related to the legacy products to provide quality products to the customer. Guide group for the smooth technology transfer of new as well as existing products or trouble shoot products for better to meet the finished product specification. Ensure the Regulatory queries to be addressed in time and guide the group leaders to work on to provide comments on the received quires to be close within provided timeline. Work closely with cross functional team for planning /execution of the Technology transfer/Exhibit/Validation batches of the individual projects to meet the timelines assigned. Provide the technical oversight (guidance), Plan, co-ordinate and oversee the work activities related to technology transfer/Exhibit batches/Validation batches of projects not limited to EU authorization but also CMO/ROW projects. Ensure Compilation of Development batches/Exhibit batches/validation batches data included with critical observations and submission of the same to R&D Head. Co-ordinate with production department for planning of tech transfer /Exhibit/Validation batches and execution/monitoring of the batches of the products starting from dispensing of the materials till packaging of the product to ensure smooth technology transfer of the products complying to the regulatory requirements. Preferred candidate profile- - 8-12 years of experience in Regulated market- OSD formulation & Development and technology transfer. - Good communication, open exchange of information and project teamwork will be required in order to meet the job performance. - Will be expected to accomplish his work assignments by interacting closely with scientific staff/Production staff and by developing the co-operative working relationships with other personnel within the company. - Must be able to work/co-ordinate with different functions within ALS and prioritize the workload to meet the predetermined timelines and need to work as a team with open communication, transparency and mutual trust. - Proper documentation pertaining to Formulation Development as per the Regulatory requirements and as per companys system.

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2 - 7 years

4 - 8 Lacs

Gandhinagar

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Role & responsibilities • To receive and understand the technology from FnD dept. • To design optimisation for process parameters & participate in the trials at R&D. • To transfer the technology from R&D to receivers site for the respective product. • To monitor the TT demo / exhibit/scale up and optimization batches. • To review the technical information sheet, product detail, raw material/accessories/ equipment requirement for plant trial/SU/Exhibit batches. • To propose and fix the batch size i.e. of the Demo, Scale up, Exhibit and Commercial based on Equipment Capacity/Qualification, Scale Up factor calculations & annual requirements. • To get involved and observe in the TT demo batch with F&D. • To take scale up batch at manufacturing locations and prepare scale up batch protocol, Scale Up Reports, MFC, Sampling Protocol, Risk Assessment etc. • To take the exhibit batches at the manufacturing locations and take care for its trouble shooting. • To prepare the summary reports. • To perform investigation for Deviation/ OOS/ OOT observed during SU/EB at plant. To prepare agency query responses.

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4 - 9 years

4 - 9 Lacs

Hyderabad

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Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. We have opening for Formulation R&D Department - oral solution exp or Injectable Experience : 2-10 Yrs Job Location: Pashamylaram - Patancheruv Job Description: Candidate must have knowledge-Literature Search, Product Development,Scale-up Batches, Characterization, Prototype Development, , Exhibit Batches, DOE Experiments , PDR Preparation & Development related documentation. Experience in US ,EU Markets .Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current C T C : Exp C T C : Notice Period: Current Designation:

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2 - 6 years

6 - 7 Lacs

Thane

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We are seeking a candidate to join Packaging Development Department, focusing on research and development (R&D) as well as commercial development, with a leading pharmaceutical company located in Thane. Job Duties & Responsibilities: R&D Activity: Perform Innovator packing material Characterization. Selection of primary/ secondary packing material for Exhibit batch packing. To perform Container closure suitability/evaluation. To review stability data and propose suitable packaging material for development study. Co-ordinating with formulation teams for packing of R&D and EB batches. Change part selection for stability loading. Initiation of SAP Code. Packing proposals for R&D studies To prepare document - Packaging material specification, MOA, PBOM, BPR, SOP, Guidelines, Equipment/instrument qualification and other documents. To initiate Change control and closure of activity. To Co-ordinate with vendor for mold development. To Co-ordinate with TTG, production, PPIC and Store team for execution of exhibit batches. Material indenting and maintaining inventory. To perform inhouse test for development of new method (MOA). Prepare and execut various studies for the determination of mechanical strength of material),protocols & reports on packing material Like MVTR study, vibration study, drop-impact study and actual simulated transit study Co-ordinating with testing lab for testing of packaging material. To develop new packaging material as per requirement. To procure new lab apparatus/ equipment. Commercial Activity: Checking of digital artwork, Print proof and shade card. Internal and External co-ordination: Internal: Packaging, Formulation, TTG, Purchase, RA, CQ, QC, BD, Accounts etc External: Packaging Material vendor, Machine vendor and other. Job Specifications: Qualification B.Pharm/B.Sc/M.Sc + PGD Packaging Years of Experience 3-5 years Previous Industry Experience Pharma Sector Working Location Thane

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4 - 9 years

4 - 9 Lacs

Hyderabad

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Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. We have opening for Formulation R&D Department - oral solution exp or Injectable Experience : 2-10 Yrs Job Location: Pashamylaram - Patancheruv Job Description: Candidate must have knowledge-Literature Search, Product Development,Scale-up Batches, Characterization, Prototype Development, , Exhibit Batches, DOE Experiments , PDR Preparation & Development related documentation. Experience in US ,EU Markets .Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current C T C : Exp C T C : Notice Period: Current Designation:

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8 - 11 years

10 - 15 Lacs

Hyderabad

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Role & responsibilities Job description Develops project plans for all aspects of assigned projects and manages all project activities Establishes and leads cross functional project teams and status meetings Obtains consensus and buy-in from key internal and external stakeholders for project timeline Monitors and manages project scope, budget, forecast, resources, and deliverables within timeline Maintains up-to-the-minute project action plans and serves as a resource to stakeholders Develops and mentors project team members Drives regular and Kick-off meetings. Performs Risk assessment of Project (Critical Aspects) Initiate the Product initiation Form (PIFs) and works closely with Head -R&D and ensures the same is approved by the Board. Provides timely, comprehensive project status reports (in form of slide decks on behalf of R&D), including budgets and timelines. Ensures all stakeholders receive the required level of detail commensurate with their role Provides input on strategic goal, tactical planning, and high-level staffing plans Proactively identifies significant project risks, develops mitigation strategies, escalates to leadership, and implements approved mitigation steps Develops and maintains subject matter expertise to effectively plan and fully execute assigned projects Manages various system-wide projects, product conversions, trials, and introduction of new products as they are assigned to R&D for start. Coordinates meetings, project teams, and working groups Closely liaise with CFTs works with them and ensures the requisites are completed before product goes for scaleup and exhibit batches. Coordinates with plant QC and production to ensure the Scaleup and Exhibit batches are timely executed. Provide a weekly update of all projects to Head-R&D. Should manage escalations effectively and converse smoothly during any conflict situation arising in his/her project review meeting(s). Should be a role model from servant leadership point of view. Raise Red Flags as and when required to Head-R&D. Should anticipate risk proactively (or failures if any in his/her project ) and build a mitigation strategy so that the project is delivered on time, as per expectation of Head-R&D. Core Competencies needed: Person should be a team player and expected to be highly calm & composed in every crucial situation arising due to inter department conflicts (if any) Excellent interpersonal skills Excellent English speaking and writing skills Excellent Presentation skills Excellent negotiations and persuasion skills Excellent conflict management skills High on company`s values and behaviours

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9 - 14 years

8 - 14 Lacs

Dahej

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Role & responsibilities: Candidate should have core experience in the field of Technology Transfer. Should have in depth knowledge about documentation, exhibit, scale up, OSD, coating, granulation and compression. Preferred candidate profile: Candidates should have experience in Pharmaceutical background. Qualification: M. PHARM. Experience: 8 to 15 Years

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3 - 8 years

2 - 7 Lacs

Dahej

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Role & responsibilities: Candidate should have core experience in the field of Technology Transfer. Should have knowledge about documentation, exhibit, scale up, OSD, coating, granulation and compression. Preferred candidate profile: Candidates should have experience in Pharmaceutical background. Qualification: M. PHARM. Experience: 3 to 8 Years

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