24 Exhibit Batches Jobs

Job Description Perform protocol for drug excipient compatibility studies and submit the protocol for review and approval Complete lab. experiment hands-on independently (Lab scale to exhibit batch and query handling). Dosage forms experience: Solid Orals Predominantly more than 90% in career. Perform formulation development activities on differentiated formulations and innovative technologies as part of product development. Carry out /Support Scientific literature search (CVM/USFDA/Daily-med/publications). Follow good laboratory practices, good documentation practices (online LNB writing) and maintain the logbooks and forms for equipment/instruments. Compilation, interpretation and review o...

Authorize to prepare and review the following documents: a. Trial Batch /Development Batch Manufacturing Record. b. Trial Batch / Scale up batch protocol & report. c. All other documents (If any) from R&D and other locations 2. Responsible for monitoring of Trial / Development / Scale up / Exhibit batches to be executed in manufacturing area. 3. Responsible to coordinate with CFT members for preparation of production plan related to Trial/Development/Scale-Up/Exhibit batches. 4. Responsible to maintain the area with GMP compliance. 5. Responsible for handling of new products from R&D and other locations 6. Responsible for handling of technical issues/OOS/Deviation investigation related to on...

Job Title: Artwork Checker Location: Thane, Maharashtra Industry: Pharmaceutical Manufacturing Department: Regulatory Affairs / Packaging Development Role Summary: We are seeking a detail-oriented and quality-driven Artwork Checker to join dynamic team of my pharma client. The ideal candidate will play a critical role in ensuring packaging artwork accuracy and compliance across domestic, regulated, and ROW markets. This position involves close coordination with cross-functional teams and supports the R&D section through RLD analysis and specification management. Key Responsibilities: Collaborate with the R&D team for Reference Listed Drug (RLD) analysis to support regulatory submissions. Per...

Dear Candidate, We are looking for formulation scientists for our Ophthalmic in Formulations, focusing on the formulation development of sterile ophthalmic dosage forms solutions, suspensions, and emulsions. This role involves complete ownership of formulation and process development with a strong emphasis on regulatory compliance and timely execution. Position: Assistant Manager Department: Ophthalmic team - Formulation Development Required Exp : 6-12years Role & Responsibilities: Formulation & Process Development Independently develop formulations for ophthalmic, injectables and nasal sprays Design and interpret DoE studies for optimization and robustness Technology & Excipient Evaluation ...

Role & responsibilities Review and provide technical inputs on Product Development Reports (PDR), Master Formula Cards (MFC), and Technology Transfer (TT) documents. Prepare product process-related risk assessments, protocols, and reports for feasibility trials and scale-up batches. Execute trial and scale-up batches, and prepare summary reports. Prepare and review Exhibit Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR). Support regulatory filing by providing intended commercial BMR, BPR, and stability evaluation summaries. Support regulatory in obtaining Test Licenses, Import Licenses, No Objection Certificates (NOC), and Manufacturing Licenses by providing the necessary...

Role & responsibilities Job Title: Sr. Executive/Executive ( 6 to 9 years of Experience ) Location : Baddi , Himachal Pradesh Key Responsibilities: 1. Technology transfer (NPD and site transfer), process validation, and continuous improvement/gross margin improvement projects. 2. Experience in product/process development for various dosage forms, including: - Solid Oral (Tablets/Capsules) - Semi- Solid dosage form - Topical (Creams/Lotions/Ointments) - Oral Liquids (Syrups/Suspensions) - Cosmetic formulation experience is a plus. Preferred candidate profile Preferred candidate profile from Solid Oral (Tablets/Capsules) - Semi- Solid dosage form - Topical (Creams/Lotions/Ointments) - Oral Liq...

Responsible to ensure Technology Transfer activities (From R&D to site, From Site to site). Manage the Scale-up, Process Optimization, submission batches, Process Validation, Process Improvements & Troubleshooting activities. Ensure timely execution of Feasibility, Assessment, Registration, New product launches and AVD projects by continuous co- ordination with unit Production, QC, ADL, RA and Project Management Team. Monitoring the progress of product status during stability study, responding the queries from various regulatory bodies. Review of Process Optimization reports. Review of gap analysis and define the action plan. To provide technical inputs for closure of OOS/OOT. Identification...

Job Description: As a Specialist in Process Development at Dr. Reddys Laboratories Ltd., you will play a vital role in the pharmaceutical development process. Your responsibilities will include conducting strategy evaluations, designing and optimizing pharmaceutical processes, calculating batch sizes, performing scale-up calculations, handling exhibit batches, and preparing technical documentation. Your expertise will ensure the successful development and scale-up of pharmaceutical products, with a focus on oral solid formulations and process validations. Key Responsibilities: - Conduct strategy evaluations to design and optimize pharmaceutical processes for efficient and cost-effective deve...

As a member of the product development team, you will be responsible for conducting literature searches, gaining a deep understanding of the product, and interpreting data for further development. Your role will involve designing primary product strategies and preparing them for discussion with group leaders or team leaders. You will be involved in planning and executing product development work to achieve the desired product profile, as well as compiling relevant data. In this position, you will be responsible for executing and evaluating various formulation optimization trials and process optimization trials, while also compiling the resulting data. Additionally, you will be required to ma...

The job involves conducting literature search, enhancing product understanding, and interpreting data for product development. You will design primary product strategies and prepare them for discussion with group leaders or team leaders. It is important to plan and execute product development work effectively to achieve the desired product profile and compile relevant data. You will be responsible for scheduling work plans in consultation with group leaders or reporting authorities to ensure timely project completion based on assigned priorities. Additionally, the role includes executing and evaluating various formulation optimization trials, process optimization trials, and compiling data. ...

You will be responsible for conducting literature searches, gaining a thorough understanding of the product, and interpreting data for product development purposes. Additionally, you will design primary product strategies and prepare product strategies for discussion with group leaders or team leaders. Your role will involve planning and executing product development work to achieve the desired product profile, as well as compiling data. You will be required to schedule work plans in consultation with group leaders or reporting authorities to ensure timely project completion based on assigned priorities. Furthermore, you will carry out the execution and evaluation of various formulation opti...

Summary Job Functions: Handling, supporting and executing all activities including training to subordinates for manufacturing process support and any late stage developmental work for process improvement related to Downstream process in MSAT. Key Responsibilities: - Execution of process scale up experiments, documentation and process improvements to support manufacturing. - Process transfer and execution of tech. transfer with help of BBM. - Planning and executing experiments of DSP for process improvement, demonstrating and recording the same in proper format / report. - Designing and execution of scale down experiments to support manufacturing for scale up. (Bag evaluation/Filter sizing/Al...

Role & responsibilities Dy.Manager / Manager Production Preferred candidate profile Responcible for Tablet Granulation, Coating & compression, Laser drilling machine , Responsible for sieve, screen, FBE finger bag inventory records, Should Have exposure with Exhibit batches, validation batches , Responsible for Production dept. and process improvement and development. Responsible for manufacturing of new products coordinating with R&D department. Resolve the Quality issues or any delay by coordinating with other departments. Preparation of Batch Manufacturing Record (BMR) from R&D guideline. Investigate the incidents and deviations in production area. Manpower handling and time management. s...

Role & responsibilities: Candidates will have to work on Apprenticeship Training for one year. If your performance is excellent we will consider you for permanent job role opportunity. Department: Formulation Technology Transfer Preferred candidate profile: Candidates should have the below mentioned % criteria: In 10th & 12th Candidate should have 60% aggregate or above of both the classes. Candidates should not have any kind of ATKT/Backlog throughout M. Pharm degree. Location: Dahej, Gujarat Stipend: Rs. 12,000 per month (Fixed) Interested candidates please share your updated CV's on hrdahej@torrentpharma.com.

Role & responsibilities: To receive instructions from AM / Manager / GM. To plan the work as per instructions from department head. To track the daily exhibit / site shift product's trail, engineering, Exhibit & Validation (not limited to) batches manufacturing and monitor it's progress constantly. To organize, supervise and control the activities of Technology Transfer department. To co-ordinate and co-operate with various departments like Raw material store, Engineering, Quality Assurance, Administration, Information Technology, Operational Project, Quality Control, Production etc. for smooth functioning of Technology Transfer department. To check and update various documents and records, ...

Role & responsibilities Job description Dosage forms experience: Solid Oral & Injectable experience in TTD/PDL/MS&T. Perform formulation development activities on differentiated formulations and innovative technologies as part of product development in R&D and in Pilot/Manufacturing Site. Follow good laboratory practices, good documentation practices (LNB writing) and maintain the logbooks and forms for equipment/instruments. Dedicate Experience in technology transfer of product(s) under development activities from scale up, exhibit batches. To lead and support the site transfer products from scale up to product launch. To prepare, review and hand-over the Technology Transfer Dossier to plan...

Great Opportunity to work with one of the fastest growing Pharmaceuticals in India!! About us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. We are expanding our team!! Looking for passionate Formulation Scientist - Technology Transfer - EU market at...

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...

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: care...

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 C...

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 timel...

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 wi...

Hello, We have urgent opening for the below profile Designation :- Executive / Asst. Mgr. - Packaging and Development - OSD Experience :- 7-9 years Educational qualification : M.Sc. M.Pharm, Diploma in Packaging Location : Mumbai Dosage forms : Oral solids Dosage Job Responsibilities :- 1. Analysis of Innovator/RLD samples for US, EU, Domestic and ROW Market. 2. Coordination for Stability packing for US, EU, Domestic and ROW Market at R & D. 3. Preparation of Container Suitability Report. 4. Development for the Suitable packaging material for solid Orals Products based on R & D Stability Data. 5. Change part development for Exhibit batches and Coordination for Machine Trial. 6. Documents Pre...

Dear Candidate, We are looking for formulation scientists for our Ophthalmic and Nasal teams in Formulations, focusing on the formulation development of sterile ophthalmic dosage forms solutions, suspensions, and emulsions. This role involves complete ownership of formulation and process development with a strong emphasis on regulatory compliance and timely execution. Position1: Assistant Manager Department: Ophthalmic team - Formulation Development Required Exp : 8-12years Position2: Research Associate/Sr.Research Associate Department: Nasal team - Formulation Development Required Exp: 4-8years(Candidates from injectables background can also apply.) Role & Responsibilities: Formulation & Pr...