41 Pharmaceuticals jobs in India
Executive - Pharmaceuticals
Posted today
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Job Description
- To perform product lifecycle management tasks for externally supplied products and own production products like evaluation of change controls, deviations, temperature excursions, stability data, process validation documents from Product quality point of view.
- Handling of problem-solving cases for products (includes both analytical and formulation related changes which have impact on product quality).
- Overall product quality evaluation and provide input during supplier's meetings.
- Follow up with suppliers and/or other stakeholders for documents related to changes for externally supplied products. E.g., possible impurities in API and finished products risk assessment in line with updated guidelines.
- Requesting, follow-up and tracking of Product Quality Review (PQRs) related data.
- Preparation and evaluation of Product Quality Review (PQRs) for externally supplied products, related coordination and follow-up with suppliers and other stakeholders.
- Writing of Product Quality Review (PQRs) for own production products and ensure its timely approval.
- Preparation and review of other documents related to Product Quality Review (PQRs).
- Responsible for planning stability studies, writing and/or review of stability protocols, reports and preparation of technical documents in CTD format.
- Co-ordinate and follow up stability studies at CROs/CQC.
- Writing and/or reviewing of process validation, technology transfer, study batch documentation for own products.
- Write/check/review pharmaceutical documents as per regulatory requirements.
- Write documents into Orion’s IT systems.
- Preparation and maintenance of lists/documents/records and archiving at appropriate place.
- Co-ordination with other departments / partners.
- Achievements of responsibilities within the agreed timelines.
- To assist the overall working of Indian Pharmaceutical team.
- Other possible tasks appointed by Supervisors.
**Note: We do not have own laboratories in India!**
**Primary Skills (essential)**
- Minimum 4 years' experience in Formulation R&D or API R&D activities in global Pharma industry
- Knowledge of organic chemistry/ Pharmaceutical medicinal chemistry/ synthetic chemistry will be an added advantage
- Ability to analyze the impact of change on Nitrosamine and/or other relevant physico-chemical risks assessment, if possible.
- Confirmed knowledge of EU requirements and ICH guidelines
- Practical development skills from the laboratory to the production scale concerning different types of formulations (tablets, capsules, liquids, etc.) will be considered as an added advantage.
- Fluency in oral and written English
- Task oriented with learning attitude and Teamwork skills
- Confirmed skills of Microsoft Office are essential
**This job offers**
- An excellent opportunity to work in an inspiring and important role in the area of Pharmaceuticals
- Great opportunity to become part of the wholly owned subsidiary of globally operating Orion Group
- Possibility to utilize your own strengths with the support of professionals
- Flexible, high spirit working environment where your skills are appreciated
- Good work-life balance
- Clear, transparent processes and responsible supervisors are our benefits to the personnel
**Education**
Bachelors/master's degree in pharmacy from a reputed College/University or
Master's degree in chemistry from a reputed College/University
At Orion, your work creates true impact and well-being for our customers, patients and society at large. Our culture of friendliness, respect, mutual appreciation and diversity creates a safe working environment where you can strive for excellence. We offer a wealth of career paths and development opportunities that support the development of innovative solutions and improving the quality of life.
- Required documents: CV/Resume
- Application deadline: 31.07.2025
Pharmaceuticals Sales Representative
Posted today
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Job Description
Samyak Herbal Health Care is an Ayurvedic Pharma Company specializing in the research and development of proprietary medicine. We are in business for more than 10 years and are looking to expand our business with direct sales in Ahmedabad. Job Overview
We are looking for an efficient and professional Pharmaceutical Sales Representative for our company.
You should be competent enough to thrive in a fast-paced business setting. You should distribute information about our products to the physicians. You should also try to convince doctors to prescribe more of our companies drugs.
You will act as a key link between a company and healthcare experts, aiming at meeting our sales targets.
If you consider yourself suitable for this Pharmaceutical Sales Rep position, please do apply. We will love to meet you.Responsibilities
Assess the client’s requirements and present them with suitable products/services.
Persuade the targeted physicians to prescribe certain products by utilizing your expert sales traits.
Provide accurate product information and deliver product samples.
Increase the visibility and awareness of the company’s medical and pharmaceutical products and maximize sales growth.
Implement brand strategies to make sure a consistent marketing message is conveyed.
Keep accurate records and documentation for reporting as well as feedback.
Build a sound relationship with the medical representatives to influence the target groups in the decision-making process.Requirements
2+ years of work experience as a Medical Salesperson, Pharmaceutical Representative or a similar role in the Pharmaceutical Industry.
Know-how of treatments along with their side effects.
Exceptional knowledge to inspect medication in various health care areas.
Excellent communication, negotiation, and sales skills.
Target driven individuals having a highly motivating sales track record will be preferred.
Proficiency in Microsoft Office.
A keen eye on details for accuracy.
Good time management skills.
Ability to work in a team or individually as and when required.
Ability to manage and handle multiple tasks.
Quality Assurance Pharmaceuticals
Posted today
Job Viewed
Job Description
- Reviewing and approving new formulations, labels, shelf life extensions, repacks and in-house preparations.
- Writing, reviewing and approving Quality documentation, including validation protocols and reports, change controls and Good Manufacturing Practice (GMP) deviations.
- Assisting with customer and product queries and complaints.Writing, reviewing and approving Standard Operating Procedures (SOPs).
- Involvement with technical customer queries and product investigations.
- Responding to enquiries in a timely manner, giving advice on ‘specials’ quality requirements in order to maintain the company's reputation for customer service and technical acumen.
- Dealing with the administration and monitoring of the QMS, including change controls, GMP deviations, technical agreements, validation reports, quality risk assessments, customer complaints, periodic reviews, self inspection and external audit reports, and SOPs.
- Conducting/assisting with internal self inspection audits.Participating in regulatory inspections.
- Ensuring that the business complies with current and future worldwide GMP standards and requirements.
- Carrying out monthly review of Controlled Drug (CD) stock checks.
- Dealing with CD related activities on site and advising the company’s Regulatory Manager of any issues with CDs.
- Delivering internal training e.g. GMP and Hygiene Induction training, Level 3 Diploma in Pharmacy Service Skills (NVQ).
- Ensuring safe working practices in accordance with COSHH.
- Ensuring good relations and communications with all members of the team and responding politely and in a timely fashion to internal and external customers.
- Working with all members of staff to maintain and develop the positive progressive culture within The Specials Laboratory.
- Observing and complying with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP).
- Observing and complying with company Health and Safety Policies.
- Observing and complying with company Standard Operating Procedures (SOPs).
**Salary**: ₹11,000.00 - ₹17,000.00 per month
Schedule:
- Day shift
Ability to commute/relocate:
- Kala Amb, Kala Amb - 173030, Himachal Pradesh: Reliably commute or planning to relocate before starting work (required)
**Education**:
- Bachelor's (preferred)
**Experience**:
- total work: 4 years (preferred)
**Speak with the employer**
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Pharmaceuticals Sales Representative
Posted today
Job Viewed
Job Description
Samyak Herbal Health Care is an Ayurvedic Pharma Company specializing in the research and development of proprietary medicine. We are in business for more than 10 years and are looking to expand our business with direct sales in Ahmedabad.
**Job Overview**:
We are looking for an efficient and professional Pharmaceutical Sales Representative for our company.
You should be competent enough to thrive in a fast-paced business setting. You should distribute information about our products to the physicians. You should also try to convince doctors to prescribe more of our companies drugs.
You will act as a key link between a company and healthcare experts, aiming at meeting our sales targets.
If you consider yourself suitable for this Pharmaceutical Sales Rep position, please do apply. We will love to meet you.
**Responsibilities**:
- Assess the client’s requirements and present them with suitable products/services.
- Persuade the targeted physicians to prescribe certain products by utilizing your expert sales traits.
- Provide accurate product information and deliver product samples.
- Increase the visibility and awareness of the company’s medical and pharmaceutical products and maximize sales growth.
- Implement brand strategies to make sure a consistent marketing message is conveyed.
- Keep accurate records and documentation for reporting as well as feedback.
- Build a sound relationship with the medical representatives to influence the target groups in the decision-making process.
**Requirements**:
- 2+ years of work experience as a Medical Salesperson, Pharmaceutical Representative or a similar role in the Pharmaceutical Industry.
- Know-how of treatments along with their side effects.
- Exceptional knowledge to inspect medication in various health care areas.
- Excellent communication, negotiation, and sales skills.
- Target driven individuals having a highly motivating sales track record will be preferred.
- Proficiency in Microsoft Office.
- A keen eye on details for accuracy.
- Good time management skills.
- Ability to work in a team or individually as and when required.
- Ability to manage and handle multiple tasks.
Deputy Manager Production (Pharmaceuticals)
Posted today
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Job Description
JOB TITLE - DEPUTY MANAGER PRODUCTION
EXPERIENCE - More than 10 years of experience in Pharmaceutical Production.
JOB RESPONSIBILITY -
Production Planning & Scheduling : Develop and implement production plans, schedules, and workflows for Specially liquid and ointment manufacturing, optimizing resource allocation and minimizing downtime
Equipment Management: Oversee the operation, maintenance, and troubleshooting of production equipment, including mixers, filling machines, and other relevant machinery.
Material Management: Ensure the proper sourcing, storage, and handling of raw materials, including liquids, ointments, and packaging materials, adhering to inventory control procedures.
Safety & Compliance: Enforce safety protocols, maintain a safe working environment, and ensure compliance with all relevant health, safety, and environmental regulations.
Team Management: Supervise and motivate production staff, providing training, guidance, and performance feedback.
Cost Management: Monitor production costs, identify areas for improvement, and implement strategies to optimize efficiency and minimize waste
Process Improvement: Identify opportunities to enhance production processes, improve efficiency, and reduce costs, implementing changes as needed.
Documentation & Reporting: Maintain accurate production records, batch records, QMS, and other required documentation, and prepare reports on production performance.
SKILLS REQUIRED -
- Proven experience in especially liquid and ointment manufacturing processes.
- Strong understanding of production planning, scheduling, and control.
- Proficiency in operating and maintaining production equipment.
- Knowledge of regulatory requirements.
- Fluent Knowledge of Word and Excel.
- Excellent leadership, communication, and interpersonal skills.
- Ability to manage and motivate a team.
- Strong problem-solving and decision-making abilities.
- Familiarity with relevant safety regulations and procedures.
- Proficient in MS Office (Word, Excel, PowerPoint)
- Follow the rules and regulations of company with respect to Health, Hygiene, safety and quality of product & personnel
SALARY -
CTC package will be suitable and negotiable based on the present package and industry norms for the right candidate.
QMS Specialist - Pharmaceuticals Manufacturing
Posted today
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Job Description
Job Summary : We are seeking a highly motivated and detail-oriented QMS professional to join our Quality Assurance team in Mendine Pharmaceuticals Pvt Ltd. The successful candidate will be responsible for ensuring compliance with regulatory requirements and company standards by implementing and maintaining effective quality management systems. This role involves managing various quality-related activities, including quality risk management, batch manufacturing record preparation, process validation, and deviation management.
Key Responsibilities :
1. Quality Risk Management:
Identify, assess, and mitigate quality risks associated with products and processes.
Implement and maintain a quality risk management system in accordance with regulatory guidelines.
2. Batch Manufacturing Record (BMR) Preparation:
Prepare and review BMRs for accuracy and compliance with regulatory requirements.
Ensure BMRs are properly approved, controlled, and distributed.
3. Process Validation:
Coordinate and execute process validation activities, including protocol preparation, execution, and reporting.
Ensure compliance with regulatory requirements and company standards.
4. Packaging Material Specification Preparation:
Develop and maintain packaging material specifications in accordance with regulatory requirements.
Ensure specifications are properly approved, controlled, and distributed.
5. Annual Product Quality Review (APQR):
Prepare and review APQRs for products, including trend analysis and recommendations for improvements.
Ensure APQRs are properly approved and distributed.
6. Cleaning Validation:
Coordinate and execute cleaning validation activities, including protocol preparation, execution, and reporting.
Ensure compliance with regulatory requirements and company standards.
7. Deviation Management:
Investigate and document deviations from established processes and procedures.
Ensure deviations are properly approved, controlled, and closed out.
8. Change Control Management:
Coordinate and execute change control activities, including assessment, approval, and implementation.
Ensure compliance with regulatory requirements and company standards.
9. Batch Card Preparation:
Prepare and review batch cards for accuracy and compliance with regulatory requirements.
Ensure batch cards are properly approved, controlled, and distributed.
10. Technology Transfer:
Coordinate technology transfer activities, including documentation, training, and execution.
Ensure compliance with regulatory requirements and company standards.
11. Coordination with RA & R&D:
Collaborate with Regulatory Affairs (RA) and Research & Development (R&D) teams on quality-related matters.
Ensure effective communication and coordination on quality-related activities.
Skill Requirements:
Master's degree in Pharmacy.
Minimum 3-7 years of experience in a QA/QMS role in the pharmaceutical industry.
Strong knowledge of regulatory requirements, including cGMP, ICH, and ISO 9001.
Excellent analytical, problem-solving, and communication skills.
Ability to work independently and lead cross-functional teams.
Salary & Benefits:
Competitive salary based on present package & industry norms.
Opportunities for professional growth and development.
Collaborative and dynamic work environment.
If you are an Eligible, motivated and detail-oriented professional with a passion for quality management, please submit your application.
Sales Manager (Export) Pharmaceuticals
Posted today
Job Viewed
Job Description
VIP Pharmaceuticals Pvt Ltd is a reputed manufacturer of high-quality pharmaceutical formulations , including tablets, capsules, oral liquids, and other dosage forms. With a strong domestic foundation, we are rapidly growing our international presence and looking for a driven and well-connected Sales Manager – Export to lead and grow our business in less regulated global markets .
Key Responsibilities- Identify and develop export opportunities for our pharmaceutical formulations—especially in semi-regulated and non-regulated markets across Africa, Latin America, Asia, CIS, and the Middle East.
- Build and maintain strong, lasting relationships with overseas buyers, agents, distributors , and government procurement bodies.
- Leverage your existing network of international buyers to generate new business leads and convert them into long-term partnerships.
- Negotiate pricing, commercial terms, and contracts to maximize profitability while ensuring regulatory and ethical compliance.
- Coordinate with internal departments (regulatory, production, quality control, dispatch) for smooth execution of international orders .
- Keep up-to-date with international market trends, competitors, and regional dynamics relevant to non-stringent regulatory regions .
- Attend global trade fairs, exhibitions, and virtual buyer meetings to promote the company's brand and offerings.
- Prepare sales plans, forecasts, and monthly performance reports for management review.
- Minimum 5–10 years of experience in pharmaceutical export sales , with a focus on non-regulated or semi-regulated markets .
- In-depth understanding of pharmaceutical dosage forms like tablets, capsules, oral liquids , and general formulation lines.
- Well-connected with international pharmaceutical buyers , importers, or government procurement officers in target countries.
- Strong understanding of export documentation, INCOTERMS, shipping procedures, and basic regulatory documentation (COPP, FSC, COA, etc.) relevant to less-regulated markets.
- Self-motivated, target-driven, and capable of working independently and with cross-functional teams.
- Excellent negotiation, communication, and relationship management skills.
- Willingness to travel internationally for business development and client meetings.
- Bachelor’s degree in Pharmacy, Life Sciences, or Business .
- MBA in International Business or similar field preferred.
- Familiarity with CRM, ERP, or export management tools is a plus.
- Competitive salary + performance-based incentives .
- Opportunity to lead and grow exports in high-potential, less-regulated markets .
- Be part of a company committed to quality, growth, and global outreach.
- Collaborative work environment with opportunities for international exposure .
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QMS Specialist - Pharmaceuticals Manufacturing
Posted today
Job Viewed
Job Description
Key Responsibilities:
1. Quality Risk Management:
Identify, assess, and mitigate quality risks associated with products and processes.
Implement and maintain a quality risk management system in accordance with regulatory guidelines.
2. Batch Manufacturing Record (BMR) Preparation:
Prepare and review BMRs for accuracy and compliance with regulatory requirements.
Ensure BMRs are properly approved, controlled, and distributed.
3. Process Validation:
Coordinate and execute process validation activities, including protocol preparation, execution, and reporting.
Ensure compliance with regulatory requirements and company standards.
4. Packaging Material Specification Preparation:
Develop and maintain packaging material specifications in accordance with regulatory requirements.
Ensure specifications are properly approved, controlled, and distributed.
5. Annual Product Quality Review (APQR):
Prepare and review APQRs for products, including trend analysis and recommendations for improvements.
Ensure APQRs are properly approved and distributed.
6. Cleaning Validation:
Coordinate and execute cleaning validation activities, including protocol preparation, execution, and reporting.
Ensure compliance with regulatory requirements and company standards.
7. Deviation Management:
Investigate and document deviations from established processes and procedures.
Ensure deviations are properly approved, controlled, and closed out.
8. Change Control Management:
Coordinate and execute change control activities, including assessment, approval, and implementation.
Ensure compliance with regulatory requirements and company standards.
9. Batch Card Preparation:
Prepare and review batch cards for accuracy and compliance with regulatory requirements.
Ensure batch cards are properly approved, controlled, and distributed.
10. Technology Transfer:
Coordinate technology transfer activities, including documentation, training, and execution.
Ensure compliance with regulatory requirements and company standards.
11. Coordination with RA & R&D:
Collaborate with Regulatory Affairs (RA) and Research & Development (R&D) teams on quality-related matters.
Ensure effective communication and coordination on quality-related activities.
Skill Requirements:
Master's degree in Pharmacy.
Minimum 3-7 years of experience in a QA/QMS role in the pharmaceutical industry.
Strong knowledge of regulatory requirements, including cGMP, ICH, and ISO 9001.
Excellent analytical, problem-solving, and communication skills.
Ability to work independently and lead cross-functional teams.
Salary & Benefits:
Competitive salary based on present package & industry norms.
Opportunities for professional growth and development.
Collaborative and dynamic work environment.
If you are an Eligible, motivated and detail-oriented professional with a passion for quality management, please submit your application.
Sales Manager (Export) Pharmaceuticals
Posted 1 day ago
Job Viewed
Job Description
Key Responsibilities Identify and develop export opportunities for our pharmaceutical formulations—especially in semi-regulated and non-regulated markets across Africa, Latin America, Asia, CIS, and the Middle East.
Build and maintain strong, lasting relationships with overseas buyers, agents, distributors , and government procurement bodies.
Leverage your existing network of international buyers to generate new business leads and convert them into long-term partnerships.
Negotiate pricing, commercial terms, and contracts to maximize profitability while ensuring regulatory and ethical compliance.
Coordinate with internal departments (regulatory, production, quality control, dispatch) for smooth execution of international orders .
Keep up-to-date with international market trends, competitors, and regional dynamics relevant to non-stringent regulatory regions .
Attend global trade fairs, exhibitions, and virtual buyer meetings to promote the company's brand and offerings.
Prepare sales plans, forecasts, and monthly performance reports for management review.
Candidate Profile Minimum 5–10 years of experience in pharmaceutical export sales , with a focus on non-regulated or semi-regulated markets .
In-depth understanding of pharmaceutical dosage forms like tablets, capsules, oral liquids , and general formulation lines.
Well-connected with international pharmaceutical buyers , importers, or government procurement officers in target countries.
Strong understanding of export documentation, INCOTERMS, shipping procedures, and basic regulatory documentation (COPP, FSC, COA, etc.) relevant to less-regulated markets.
Self-motivated, target-driven, and capable of working independently and with cross-functional teams.
Excellent negotiation, communication, and relationship management skills.
Willingness to travel internationally for business development and client meetings.
Preferred Qualifications Bachelor’s degree in Pharmacy, Life Sciences, or Business .
MBA in International Business or similar field preferred.
Familiarity with CRM, ERP, or export management tools is a plus.
Why Join VIP Pharmaceuticals Pvt Ltd? Competitive salary + performance-based incentives .
Opportunity to lead and grow exports in high-potential, less-regulated markets .
Be part of a company committed to quality, growth, and global outreach.
Collaborative work environment with opportunities for international exposure .
Deputy Manager Production (Pharmaceuticals)
Posted 1 day ago
Job Viewed
Job Description
EXPERIENCE - More than 10 years of experience in Pharmaceutical Production.
JOB RESPONSIBILITY -
Production Planning & Scheduling : Develop and implement production plans, schedules, and workflows for Specially liquid and ointment manufacturing, optimizing resource allocation and minimizing downtime
Equipment Management: Oversee the operation, maintenance, and troubleshooting of production equipment, including mixers, filling machines, and other relevant machinery.
Material Management: Ensure the proper sourcing, storage, and handling of raw materials, including liquids, ointments, and packaging materials, adhering to inventory control procedures.
Safety & Compliance: Enforce safety protocols, maintain a safe working environment, and ensure compliance with all relevant health, safety, and environmental regulations.
Team Management: Supervise and motivate production staff, providing training, guidance, and performance feedback.
Cost Management: Monitor production costs, identify areas for improvement, and implement strategies to optimize efficiency and minimize waste
Process Improvement: Identify opportunities to enhance production processes, improve efficiency, and reduce costs, implementing changes as needed.
Documentation & Reporting: Maintain accurate production records, batch records, QMS, and other required documentation, and prepare reports on production performance.
SKILLS REQUIRED -
Proven experience in especially liquid and ointment manufacturing processes.
Strong understanding of production planning, scheduling, and control.
Proficiency in operating and maintaining production equipment.
Knowledge of regulatory requirements.
Fluent Knowledge of Word and Excel.
Excellent leadership, communication, and interpersonal skills.
Ability to manage and motivate a team.
Strong problem-solving and decision-making abilities.
Familiarity with relevant safety regulations and procedures.
Proficient in MS Office (Word, Excel, PowerPoint)
Follow the rules and regulations of company with respect to Health, Hygiene, safety and quality of product & personnel
SALARY -
CTC package will be suitable and negotiable based on the present package and industry norms for the right candidate.