Featured Post

OOS Investigation Tools: Streamlining Out-of-Specification Investigations

by
OOS Investigation Tools: Streamlining Out-of-Specification Investigations Out-of-specification (OOS) events are critical occurrences in pharmaceutical manufacturing, representing deviations from established specifications and potentially impacting product quality and patient safety. Efficient and thorough investigations are crucial to identify root causes, prevent recurrence, and ensure product compliance. This post explores essential tools that streamline OOS investigations. Key Tools and Examples of OOS investigation Tools: 1. Electronic Data Capture (EDC) Systems:   These systems are crucial for managing clinical trial data, but their principles of data integrity, audit trails, and secure storage are highly relevant to OOS investigations. Veeva Vault EDC: Veeva is a well-established name in the life sciences industry. Vault EDC is a cloud-based platform specifically designed for clinical data management. Its features like audit trails, electronic signatures, and version contro...
0

Amneal Pharma - Walk in - 15th Mar'20 at Panchkula AMNEAL PHARMACEUTICALS PRIVATE LIMITED

by




Amneal India walk in interview 2020

Amneal Walk in Job Requirements

  • 2 - 7 Years of experience
  • 100 Vacancies available 
  • Ahmedabad(Moraiya)
Dosage form-
parenteral, usfda, Vial, documentation, sterile, quality procedures, Ophthalmic, production department, pharma

Job Responsibilities Required

Company looking for competent, dynamic and varstile candidates for Injectable unit for Ahmedabad SEZ Matoda Plant.

Date: 15th Mar, 2020 (Sunday)
Timing: 9:00 AM to 4:00 PM

Venue :
WHRamgarhHeritage , Panchkula,
Address: The Quila, NH-73, near Sector 28,Ramgarh, Haryana 134111

INJECTABLE REQUIREMENT

Sterile Manufacturing ( Injectable unit /Parenteral Unit)

Designation: Executive/ Sr. Officer/ Officer/ Operators
Qualification: M. Pharm/ B.Pharm/ Diploma Engineering/ D. Pharm/ B.Sc/ ITI
Total Experience: 02 to 07 years
Area: Ophthalmic, Vial, PFS, LYO
Required Job specifications: Aseptic area, Controlled area, Sealing, Filling, capping, Production QMS
Position: Officer: 30
Operator: 75 
Sponsored Searches
3.    Dissolution & Related Technical Questions – By Bhagyashree Chothe
4.    What is bowie-dick test? - By Prashant Devmore
Desired Profile:
  • To observe & follow all rules and regulations of the production department.
  • Must be from Parenteral background
  • To be aware and responsible for achieving quality objective and fulfilling the requirements of the quality of the company's service by means of applicable quality procedures.
  • Sound technical knowledge of Aseptic area and controlled are related activities.
  • Technical exposure and expertise on vial filling, sealing, Autoclave, Lyophilizer, PFS filling, cartridge filling machine.
  • Knowledge of Regulatory guidelines and exposure of USFDA audits.
  • Knowledge of Eye drop filling machine and related batch mfg. process.
  • Knowledge of Quality Management System (QMS) i.e. change control, Deviation, CAPA, and documentation in manufacturing area of injectable.
  • Expertise in batch manufacturing and preparation related activities.
  • Knowledge of equipment validation and qualifications in injectable.
Required Candidate profile:
The candidate with good communication and inter personal skills, computer knowledge and exposure to cGMP/ GLP Knowledge and understanding of regulatory requirement is essential.

 Note : Candidate should have 02 to 07 years of relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organisation. You may walk in for interview with updated CV along with CTC proof, Appointment letter, Increment letter & last 3 months salary slip & Bank statement, Aadhar & PAN card and 2 passport size photograph.

If you are unable to attend interview you can share cv onneha.modi@amnealindia.com orkishan.soni@amnealindia.com

Comments

Post a Comment

If you have any doubt please let me know. Thank you.