Sun Pharmaceutical Released Job Openings On 02/02/2022. Sun Pharma beginnings in 1983, Sun Pharma has grown to become the 5th largest generic pharmaceutical company in the world and No. 1 in India. Application form link provided at the end of post.

Vacancy Details:

Sun Pharmaceutical Recruiting M.Pharm/Bachelor’s degree candidates with 1+ Years experience for Professional Medical Representative/Sr Off-Production/Exe-Maintenance/CMC QA – Team Member/Sampling Anayst/Coordinator, Pricing/Junior Officer – Production position.Complete Details for the Professional Medical Representative/Sr Off-Production/Exe-Maintenance/CMC QA – Team Member/Sampling Anayst/Coordinator, Pricing/Junior Officer – Production as follows.

Important Details :

• Location:Mohali – Plant/Gurgaon – Office/Madhurantakam
• No of Vacancies:NA
• Details of Salary:NA
• Opening date for online Application: 02/02/2022
• Mode of application :Online
• How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps

Related Job : QA,QC,R&D,Production,Sales,Packing,RA,Engineering,Medical Coding,Purchase,StoresJobs At Hyderabad,Bangalore,Vizag,Ahmedabad,Mumbai etc

Job Description/Skills Required

 Professional Medical Representative

JOB RESPONSIBILITIES

• Ensure that sales targets are achieved through effective and efficient promotion of ethical products to physicians of target specialties.
• Partnering with the customers by providing value added services.
• Plan, organize and execute product presentation to physicians and pharmacists regarding the therapeutic use of the product, mode of action, features and benefits;

JOB REQUIREMENTS

• Candidate must possess at least a Bachelor’s Degree, Marketing, Pharmacy/Pharmacology, Nursing or equivalent.
• At least 1-3 year(s) of working experience in Pharma sales is required for this position.
• 1-4 Yrs Experienced Employees specializing in Sales – Retail/General or equivalent.
• Experience in handling CNS product (Neuro and Psych) is an advantage.

Sr Off-Production

• To follow the Current Good Manufacturing Practices and all the relevant SOPs in production planning.
• To follow the gowning procedure as per the respective SOP and maintain good personal hygiene.
• To prepare the monthly production schedule for manufacturing and packing by coordinating with concerned persons, basis on RFC (Rolling forecast) received from GSC team. 
• To achieve production plan, schedule the plan in line with optimum capacity, material availability and marketing priorities & monitoring of all the scheduled activities on daily basis.
• To release the plan on weekly basis monitor the plan on daily basis.
• To conduct the weekly performance review meetings.
• To create and release the process order for manufacturing and packing.
• To have effective coordination with GSC, Production, MSTG, QA, QC, RA, warehouse & GMS for achieving the production schedule.
• To review change controls related packing materials A/W for any new material code or any revision in-between as a planning person.
• To create materials reservations related to RM/PM.
• To prepare the daily, weekly, monthly (MIS) reports.
• Issuance of forms as per SOP.
• To initiate request for Material code to code transfer.
• Review and approval of Standard operating procedure.
• Handling of Planned and Unplanned deviation, Investigation and Change control. Implementation of corrective and preventive action. Verification of effectiveness of the corrective and preventive action

 Exe-Maintenance

• Responsible for utilities, air conditioning & maintenance of building &   premises, maintenance of production, engineering equipment.
• To ensure the engineering activities such as PLC,s HMI,s  Programming Uploading Downloading, preventive maintenance, Routine & breakdown maintenance, Calibration, Equipment & area validation are carried out as per the schedule.
• To enforce and maintain high degree of morale, discipline amongst the team.   
• To ensure that all the system and equipment are upgraded, validated & Automated as per the procedures & requirements.
• To ensure that the subordinates are adequately trained for job assigned.
• Optimum utilization of resources.
• To ensure that optimum resources such as man, material & area are available for the smooth operation of engineering related activities.
• In-House training of all the persons working in the maintenance.
• Validation & qualification of all equipment/system of utilities and air conditioning.
• To ensure that contactors are trained for the job they are doing.
• Preparation & revision of SOP’s related to engineering activities.
• To ensure that all SOP related to engineering are being followed.         
• To ensure and improve machine performance on automation and regular basis. Automatic and instrumentation breakdown minimization, increasing the productivity and efficiency.
• Organize, assign and approve trainings of SOP and Topics (Regulatory, SPIL specific, Activity Based, EHS & Developmental) for Engineering Department in Learning Management System as Departmental training coordinator.

CMC QA – Team Member

1) This position is accountable for developing procedures / system and for assuring compliance to them by the R&D function.

2) Ensure the Compliant Development of New Drug Application, New Drug Delivery system, Drug Products formulations and technology transfers to the manufacturer organisation.

3) To review and approve Method Development/Method Validation / Method verification/Method Equivalency / Method Transfer data for its adequacy, accuracy and completeness as per regulatory and business requirement for intermediate, drug substances, drug products (i.e. Solid oral Tab / Cap / PFOS etc.) in order to achieve robust method development and to decrease method failure at site.

4) To support on pharmacopoeia updates and new regulations for Analytical Development Department in order to ensure continual improvement in the quality system.

5) To review and approve QMS documents i.e. change control, deviation, equipment qualification (IQ/OQ/PQ), OOS, OOT, CAPA and conducting audit for cGxP compliance.

6) Assure that formulation process packages are reviewed adequately within the team to verify scientific rigor, adequacy, and completeness (Pre formulation data, Product quality risk assessment, stability data and trend interpretation, RLD data, suitability of test with reference product, product quality specification etc).

7) Must have strong interpersonal and communication (written and spoken English) skills.

8) Must have excellent negotiation and interpersonal skills and ability to communicate effectively with all levels of the organization and external stakeholders.

9) Work effectively in an international multicultural matrix organization is strongly preferred.

Sampling Anayst

• Sampling of Raw Material, Intermediate, Finished Product.
• Carrying out validation sampling.
• Environmental monitoring.
• Instrument calibration.
• Sample registration and entry in LIMS.
• Other activities entrusted from time to time.

 Coordinator, Pricing

• Provide expertise in preparing competitive bids and create responses to RFIs and RFPs.  Ensure the processing of all contractual obligations in accordance with agreed upon terms and conditions.
• Perform data driven analysis and modeling on significant amounts of data across all financial sales functions including competition, market share, utilization, costs and other appropriate aspects for purposes of turning it into actionable information.
• Analyze, Review, make recommendation, and execute customer pricing strategies and rebate structures using historical sales trends, IMS prescription trends, market intelligence, and other pertinent information.
• Ensure all bids/offers to Customers, including terms and conditions, contract awards, and procedures to ensure internal notifications are received by appropriate personnel.
• Working in conjunction with Sales team; follow-up with all customers after bid submission to ensure the customer has received the bid, understands the offer, and to determine the company’s competitive position.
• Complete ad-hoc analyses and projects per Management’s request.  Review and address interdepartmental requests for product or customer contract information.
• Extract data from various databases using Business Intelligence tools and manipulate data using advanced Excel features such as Vlookup, Pivot Tables, etc.
• Assist in implementing bid management tool for contract management.
• Work closely with Finance and Pricing team to ensure all discounts and rebates are appropriately captured and accounted in SAP pre and post-closing; Assist in maintenance of Gross-to-net Rates.
• Assist in preparing department and customer communications.
• Work with the business lead, clients, and legal teams on contract term updates. Ensure all contracts are reviewed, red-lined, and revised for compliance.
• Manage contracts and pricing. Analyze contracted product performance and communicate account performance.
• Research and resolve price discrepancies with Accounts Receivable and Customer Service

Junior Officer – Production

1. Responsible to maintain an optimum level of manpower and over time
2. Responsible to ensure all operation of production adherence to cGMP compliance
3. Responsible on manpower development (training) for quality, productivity and cost consciousness
4. To train the production personnel on cGMP Trend & regulatory requirement.
5. Monitor the work of subordinates and ensure that the necessary assistance is provided to them for their timely, adequate and accurate completion of the assigned work
6. Accountability to ensure production planning & timely delivery of high productivity and low cost products and with compliance to cGMP.
7. Responsible for handling CAPA, Deviation, Change Control, URS, Contingency Plan and Investigation report.
8. Responsible for Departmental Standard Operating Procedure update and revision execute within production in DCM.
9. Responsible to carry out production operation as per production plan and delivery on time.
10. Other instruction by superior.