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Planning PCM/MD Specialist


Cairo, IL 62914
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Job Details

**Position Purpose:**

+ This position provides professional support for the supply chain - supply planning function encompassing coordinating products'-related change management including and not limited to labeling updates & materials source changes driven by supply chain along with master data updates.

**Primary duties:**

+ Comply with GMP requirements (WHO GMP along with Pfizer Quality Standards) in terms of bill of materials (BoM) updates, compliance, completion & review as per site quality procedures.

+ Work with the supply planning manager to ensure that PGS Cairo & External Supply Parties (i.e. CMOs) delivers on external expectations of supply to local market.

+ Responsible for coordinating the process of products'-related change management across all departments/network to ensure timed execution & implementation of the required updates/changes which is critical for a consistent products supply. Examples for product change management include and not limited to artwork changes & APIs source changes driven by Pfizer.

+ Responsible for coordinating internally within supply chain department quantity ordered/ consumption rate for the exiting stocks of old labeling in a way complying with MoH/Pfizer expectations.

+ Initiate requests related to new EnterpriseOne codes and ensure that the newly requested codes are effective.

+ Execute all requested changes related to bill of materials (BoM) and coordinate with procurement, finance, & quality to get these changes effective.

+ Ensure data integrity alignment across different systems.

+ Support supply planning manager with data analytics related to actual demand patterns vs. forecast, phased production budget vs. achieved production, slow moving inventory of both Finished Goods and materials whenever needed.

+ Prioritize effectively to ensure that time & resources are optimized to support PGS Cairo mission.

+ Initiate & participate in continuous improvement projects.

+ Develop & maintain the required standard operating procedures in accordance with corporate and regulatory requirements as they relate to GMP and production processes.

+ Prepare and report on key performance indicators and departmental activities as required.

+ Prepare all required reports needed to support other departments' data analyses.

+ Comply with all completion timelines such as and not limited to change requests, quality investigations, actions, documentation updates, & training.

**Key outputs include:**

+ Compliance: deviations, CAPA, Change Control, & Procedures.

+ Planning: timed completion change controls, & minimizing rejected stock due to old artwork.

**Technical Skills:**

+ Experience working in a pharmaceutical manufacturing site

+ Lean Six Sigma tools and methodologies


+ Bachelor's degree in a related technical or business discipline.

**Knowledge & Experience:**

+ At least 5 years directly related experience in pharmaceutical operations.

+ Understanding of GMPs and compliance in the pharma industry

+ Business acumen to operate within a large multi-national company

+ Knowledge of site operational activities

+ Strong knowledge of and commitment to Quality and EHS

+ Leadership Skills:

+ Decisive: Manage complexity to make timely, informed decisions

+ Focused: Develop impactful short and long term solutions for our customersand patients

+ Connected: Collaborate with others to accomplish shared goals

+ Inspiring: Motivate and develop self and others to drive the business forward

+ Courageous: Consistently demonstrate accountability and integrity inthe face of challenges

+ Resilient: Respond to change with agility, optimism and innovation

+ Strong organizational and planning skills, as well as a high energy level and initiative

+ Excellent verbal, written and interpersonal communication skills. English fluency is a pre-requisite,

+ Understanding of pharma commercial business

+ Analytical skills, strategic thinking and problem solving skills are a must.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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