• To give Area /Equipment clearance i.e. checking and approval of all manufacturing & filling. To verify environmental condition i.e. Temperature, Relative Humidity & Pressure Differential condition in all for said areas…
The Medical Advisor leads the execution of communication plans and marketing strategies that promote medical science. Provides assistance and direction on guidelines for new product development. Possesses a detailed unde…
Skills: Medical Marketing, Clinical Program Design, KOL Relationship Management, Pharmacovigilance, New Product Development
"• To ensure smooth and efficient functioning of plant machineries at main Pharma block. • To attend routine breakdown maintenance of production machinery of main pharma block. • To attend the modification and developmen…
Principal Tasks: To analyse finished goods, semi-finish and In-process samples. Analytical result recording in LIMS and SAP. Specification, Master, Record of Analysis preparation/correction in LIMS. Responsibilities: Spe…
Skills: LIMS, SAP, HPLC, Analytical Chemistry, Quality Control
Major Purpose Of The Job:- To follow cGMP as per training guidelines from the premises to their section. To follow the respective equipment SOP’s and written procedure from BMR To ensure environmental condition of Compre…
Skills: cGMP, SOP Adherence, BMR Documentation, Equipment Maintenance, Quality Control
Production : • To take instruction from plant-in-charge for batch charging / monitoring • To report any deviation / discrepancy in plant / process to plant in charge • To ensure completion of batches as per production pl…
Receipt of Raw Material for main Pharma stores. • SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. • To check the environmental parameters like Temperature, RH, pressure dif…
Skills: SAP, Inventory Management, cGMP Compliance, Warehouse Operations, Material Reconciliation
• Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of raw material on non-chromatographic instrument such as FTIR, UV, Polarimeter, KF, Autotitrator etc. by following test procedure. • To att…
To maintain and adherence of the GLP and safety procedures in laboratory.To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packing materials/intermediates…
Skills: HPLC Analysis, GLP Compliance, CFR 21 Part 11, LIMS, Stability Study
Job Description: Designation: Deputy Manager Department: Sales & Marketing-API (Domestic/International Market) Business Unit : CSBU Core Job Overview A professional in this role bridges the gap between technical chemical…
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process conditions for batch as per …
Skills: Production Monitoring, cGMP Compliance, Documentation, Equipment Calibration, Safety Management
Role Objective: - 1.Operating machines and ensuring the cGMP compliance in primary packing almac machine area area Key Responsibilities: •To check and ensure proper operation of the machine in his respective area. •To ma…
Principal Tasks and Responsibilities: Effective Promotion of company’s products to achieve the Sales Budgets assigned to your territory Implementing market & business strategy designed by the management Providing feedbac…
Role Objective:- Manages, implement and administer Sales and Marketing activities. Largely involved in formulating Sales and Marketing plans, guidelines, policies and short-term strategies as well as setting goals and ta…
Plan, coordinate, and monitor daily production activities to achieve monthly and annual production targets. Ensure manufacturing operations are executed in accordance with approved Batch Manufacturing Records (BMRs), SOP…
Skills: API Manufacturing, cGMP Compliance, Production Planning, Batch Manufacturing Records, CAPA Implementation
. Achievement of Targeted Business Volumes • Achieve overall monthly and annual sales targets for the assigned region. • Deliver brand-wise sales targets with special attention on Focused & New brands. • Ensure achieveme…
1. Alternate Vendor development 2. Rate approval for packing materials 3. Procurement of Corrugated boxes 4. MDM approval for new materials, New vendor Creation
Skills: Vendor Development, Procurement, Rate Approval, Master Data Management, Material Sourcing
Safety : • Assist to collect safety information. • Maintain the record of MSDS. • Support for the safety activities to colleagues. • Issue of PPE to plants as per requirement. Maintain the consumption records as per SOP,…
Skills: EHS Compliance, Occupational Health and Safety, Effluent Treatment Plant Operation, Accident Investigation, Risk Assessment
Role Objective: The incumbent will be responsible for achieving area sales targets by leading and developing a team of Field Officers, strengthening customer (KOLs, doctors, chemists) relationships, ensuring product and …
Skills: Sales Target Achievement, Team Leadership, KOL Management, Key Account Management, Pharmaceutical Sales
Principal Tasks and Responsibilities: Effective Promotion of company’s products to achieve the Sales Budgets assigned to your territory Implementing market & business strategy designed by the management Providing f…
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Full-time
Posted 16h ago
~40 hrs/week
Responsibilities
The Technical Supervisor is responsible for overseeing manufacturing and filling clearances, monitoring environmental conditions, and ensuring sterilization and lyophilization cycles are completed. They also perform product sampling, leak tests, and conduct detailed reviews of Batch Manufacturing Records for accuracy and compliance.
Requirements
The candidate must be able to execute technical procedures according to SOPs and MMD-I guidelines. They must possess the ability to review technical logs and release batches for further processing based on strict quality standards.
Full job description
To give Area /Equipment clearance i.e. checking and approval of all manufacturing & filling.
To verify environmental condition i.e. Temperature, Relative Humidity & Pressure Differential condition in all for said areas are within acceptable range at all the time during operation throughout the shift. To ensure daily verification of weighing balance with standard weights. To ensure sterilization cycles completion as per loading pattern & SOP. To ensure lyophilization cycles completion as per MMD-I & SOP.
To perform filled volume & weight method and leak test as per MMD-I & SOP.
To perform sampling of bulk and finished product for each batch at the end of the batch as per SOP entry into sampling log and submit the samples to QC for analysis.
Record review,
To review the Batch Manufacturing Records for on line entries at each stage. To review sequential log of machines. To review environmental condition records. To review of area cleaning logs.
To release the batches for further processing.
To review and checking Batch Manufacturing Records for reconciliation, correct entries, completeness, affixing of release status labels.
Founded by Shri I.A. Modi, Cadila Pharmaceuticals Ltd. is one of the largest privately held pharmaceutical companies in India, headquartered at Ahmedabad, in the State of Gujarat. Over the last seven decades, the company has been developing and manufacturing pharmaceutical products in India and selling and distributing these in over hundred other countries around the world.
Focused strongly on Innovation and Research, the company is present in more than forty-five therapeutic areas spread across twelve specialities, including cardiovascular, gastrointestinal, analgesics, haematinics, anti-infectives and antibiotics, respiratory agents, antidiabetics and immunologicals.
At Cadila Pharmaceuticals, Research and Development is at the core of all its initiatives, be it Biotechnology, APIs, Formulations, Plant Tissue Culture or Phytochemistry.
More than 300 scientists in its various Research and Development setups reinforce the competitiveness of research in the therapeutic areas which have high unmet medical needs.
Cadila Pharmaceuticals Excellence in manufacturing facilities is central to Cadila Pharmaceuticals. The company’s formulations manufacturing plant at Dholka near Ahmedabad, Gujarat is spread over hundred acres of land. This state-of-the- art facility is not only impressive in size, but is also USFDA approved.
The second formulations manufacturing facility is located at Samba in Jammu and Kashmir. The facility meets most of the stringent quality standards across the globe to produce tablets, capsules, soft and hard gelatin capsules, liquids and orals.
Two Active Pharmaceutical Ingredient (API) manufacturing units at Ankleshwar, Gujarat manufacture a wide range of APIs and intermediates including many USFDA-certified products.
The company has strong foothold in the African continent through its formulation manufacturing facility at Addis Ababa in Ethiopia.
For more information visit: https://www.cadilapharma.com/
Founded by Shri I.A. Modi, Cadila Pharmaceuticals Ltd. is one of the largest privately held pharmaceutical companies in India, headquartered at Ahmedabad, in the State of Gujarat. Over the last seven decades, the company has been developing and manufacturing pharmaceutical products in India and selling and distributing these in over hundred other countries around the world.
Focused strongly on Innovation and Research, the company is present in more than forty-five therapeutic areas spread across twelve specialities, including cardiovascular, gastrointestinal, analgesics, haematinics, anti-infectives and antibiotics, respiratory agents, antidiabetics and immunologicals.
At Cadila Pharmaceuticals, Research and Development is at the core of all its initiatives, be it Biotechnology, APIs, Formulations, Plant Tissue Culture or Phytochemistry.
More than 300 scientists in its various Research and Development setups reinforce the competitiveness of research in the therapeutic areas which have high unmet medical needs.
Cadila Pharmaceuticals Excellence in manufacturing facilities is central to Cadila Pharmaceuticals. The company’s formulations manufacturing plant at Dholka near Ahmedabad, Gujarat is spread over hundred acres of land. This state-of-the- art facility is not only impressive in size, but is also USFDA approved.
The second formulations manufacturing facility is located at Samba in Jammu and Kashmir. The facility meets most of the stringent quality standards across the globe to produce tablets, capsules, soft and hard gelatin capsules, liquids and orals.
Two Active Pharmaceutical Ingredient (API) manufacturing units at Ankleshwar, Gujarat manufacture a wide range of APIs and intermediates including many USFDA-certified products.
The company has strong foothold in the African continent through its formulation manufacturing facility at Addis Ababa in Ethiopia.
For more information visit: https://www.cadilapharma.com/