Assistant Manager - QC (Karachi, Sindh, PK, N/A)

We are Reckitt

Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.

​Research & Development​

In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.

We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.

The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.

About the role

The scope of the job includes analytical work, associated documentation and compliance to GLP. Quality Control Executive has direct reporting to the Quality Control Lead Healthcare

Your responsibilities

• • Testing of bulk, finished products & stability samples as per approved methods and performed status labelling accordingly
  • Maintaining raw data of all testing in logbooks as per SOP
  • Maintain analytical results in Batch Analytical Record Sheet as per procedure
  • Review and maintaining analytical results in Batch Analytical Record Sheet as per procedure
  • Maintain equipment usage, preparation of reagents, volumetric solution standardization logbooks
  • Perform and maintain record of Equipment Calibration
  • Keep and use copies of all approved test methods, monograph etc. available and easily accessible to perform related activities.
  • Perform Validation of non-pharmacopoeia methods
  • Preparation of stability schedule, protocols and reports
  • Preparation and validation of stability indicating methods
  • Perform regular & on-going stability testing & analysis of samples from new source
  • Ensure GLP/GMP and GDP during internal / external audit as per plan
  • Provide QC support in process validation, cleaning validation & water system validation & other projects as per plan
  • Development / simplification of analytical methods
  • Participate in investigation of OOS results
  • Write and update laboratory related SOPs
  • Troubleshoot testing failures
  • Follow all related SOPs while performing any activities within the lab.
  • Keep the specifications & Test methods aligned with latest pharmacopeia
  • Coach and mentor junior employees; seek opportunities to grow leadership in others
  • Perform any other job assigned by line manager
  • Ensure compliance & contribute to upkeep and improvement of Health, Safety & Environmental corporate policy/procedures & applicable legal requirements
  • 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 Laboratory
  • Maintain good housekeeping in the lab.

The experience we're looking for

• Bachelor’s/Masters Degree in Pharmacy (Post Graduate Degree is preferable) with at least 3-5 years of experience working in a quality and or regulatory compliance function in a Healthcare, Pharmaceutical, or related industry.
• Clear understanding and ability to assess and act upon product safety, quality, efficacy and compliance risks.
• Good understanding of typical regulatory requirements relevant to a regulated product e.g. Drugs Act 1976, DRAP Rules 2012 and GLP.

The skills for success

Commercial Awareness, Business Partnership, Collaboration, Partnership building, Ability to challenge the status quo, Propose improvement, Accountability, Adaptability, Collaborator, R&D, Product Lifecycle Management.

What we offer

With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.

Equality

We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.