Unison Pharmaceuticals - Urgent Openings for Quality Control / International Business Development

Unison Pharmaceuticals - Urgent Openings for Quality Control / International Business Development


Department: Quality Control For QMS Investigator
Position: Executive / Sr. Executive

Key Accountabilities / Responsibilities:
1. To raise QMS related documents like, Deviation, Out of specification, Out of trend results observed.
2. Prepare the Investigation report along with QA representative and execution immediately.
3. Prepare the summary report and trend of QMS data.
4. Ensure that, closing of Deviation within time frame as well as CAPA closer within predefined Targeted date (TCD).
5. To follow Good laboratory practices (GLP), Good documentation practices (GDP) and safety precautions during routine analytical activities.
6. Ensuring good relations and communications with all members of the team and responding politely and in a timely manner to internal and external customers.
7. Working with all members of staff to maintain and develop the positive progressive culture within the laboratory.
8. Any other additional responsibility given by Section In-charge.
9. Candidates should also have sound knowledge of cGMP documentation and must be familiar with cGMP requirements.

Note: Interested candidates may also email their resume to career@unisonpharmaceuticals.com

Department:  International Business Development 
Position: Executive/Sr. Executive

Key Accountabilities/ Responsibilities: 
1. Potential client identification & business collaboration
Identify the potential client by analyzing IMS/ export-import (EXIM) data / social networking sites for assigned territory of European countries along with point of contact.
Preparing customer profile for senior leadership approval before contacting customers
Share corporate presentation via e-mails, telecons to customer to promote CMO / CDMO / OL business models and collect forecasts for interested products
Follow up on new projects with existing customers along with internal confirmation on IPR & RA aspects
Prepare costing required sheet and collect / evaluate commercial proposal for sharing with customer
Follow up & negotiate on commercial proposal, agreement drafts in co-ordination with legal team
Preparing DRF and arrange dossier audit as per customer requirement for due diligence in co-ordination with RA team.

2. CMO
Hosting telecons with both internal & external stake holders to facilitate the discussion on gap analysis / challenges.
Coordinate with internal stake holders for timely completion of feasibility trails, validation batches and commercial batches.
3. CDMO/out-licensing
Arrange the product-wise SOW (Scope of Work) which majorly includes milestones payment, product forecast & associated development cost.
Tracking of projects & arranging stake holders feedback / approval where-ever necessary
Follow up internally for additional cost incurred & negotiating with customer for absorbing the same
Creating milestone / pass thru cost invoices, sharing with customers & follow up on payments.
4. Market intelligence and data analysis
Understanding competitors and business trend in market for Unison portfolio by analyzing IMS / EXIM
Evaluating potential business from new products (Oral solutions & Capsules) using IMS data.
5. Backend activities
Order Management
PO acknowledgement to customer; check batch size & COGS in line with agreement
Cross-check with finance for profitable COGS in current scenario.
EOC drafting & initiation
Gather comments from RA /PD /QA for MA, variation approval, artworks, FG codes
Sharing updated EOC across internal stake holders for review & signing
Follow up with Purchase, PPMC & Production for OTIF delivery.
Customer relationship management with real time updates & telecons on challenges
Follow up with customer on pick up of goods and payment receipt against open invoices.
6. MIS activities
Maintain masters for Orders and License Fee / Pass thru costs
Compiling EOCs, Tracking open invoices, payment due dates & receipts
MPRM report preparation
SnOP report preparation
Weekly BD report on lead generation status.
7. SAP activities
Business partner creation
Goods & Service order Booking / Reversal / Cancellation
Service Invoice / credit note issuance & printing
Follow up internally on FG / SFG code creation in SAP
Validation of new functions in Development / Quality server.
Note: Interested candidates can share their resume to career@unisonpharmaceuticals.com

Comments

Similar Jobs

Dr. Reddy’s – Walk-In Interviews on 26th March 2023

ZYDUS – Walk-Ins - for Multiple Positions - in Production, QC, QA, Microbiology, Warehouse, Engineering - on 2nd Apr’ 2023

Mylan Laboratories Ltd - Urgent Hiring for Manufacturing / QA

APL Health Care Ltd (Aurobindo) – Walk-In Interviews for Multiple Positions on 5th August’ 2023

Claroid Pharmaceuticals Walk-in Interview on 1st Jan.2023

Gufic Biosciences Limited – Urgent Openings for QC / QA / QC-Micro / Warehouse / Stores – Apply Now

Intas Pharmaceuticals – Walk-In Interviews for - Freshers & Experienced Candidates on - 20th & 21st Apr’ 2023

ELICO Healthcare – Walk-In Interviews on 1st – 9th Sep’ 2023 for Freshers & Experienced in Quality Assurance

Immediate Openings for Quality Control / Production / Solvent Recovery / HVAC - Bulk Drug Plant @ BVR Solutions, Hyderabad

Biological E. Limited – Walk-In Interviews for FRESHERS on 17th & 18th Aug’ 2023