한국약대 다니고 대학원도 아마 한국에서 다닐거같은데 캐나다 제약회사 들어가려면 조건이 어떻게되나요?

일반적으로 캐나다에서 취업은, 기업이 직원이 필요하게 되면, 공고를 내고, 1~2주 정도내에 이력서 접수를 받은 다음, 5~10명 정도 면접 대상을 선정하고, hiring manager (직원이 필요한 곳의 매니저 = 보통 한국으로 치면 "부장"이나 딱 부장만 면접을 진행하지는 않음, supervisor나 VP나 아무나 자기 밑에 사람 뽑는 사람을 하이어링 매니저라고 함)가 면접을 진행해서 마음에 드는 놈으로 고릅니다.

회사마다, 자리마다, 직책마다 조건은 모두 다르고, 거기에 맞게 이력서 작성해서 면접 (보통 영어) 1시간 정도 해서 취업하는게 일반적입니다.

https://www.pfizer.com/about/careers Careers | Pfizer

Careers Menu Home About Careers This is where today’s pioneers, problem solvers, and pathfinders meet to create tomorrow’s breakthroughs. Together, we can transform patients’ lives. Play Video (Opens in a new window) Benefits Pay for Performance Philosophy and Practices Pfizer structures its compens...

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파이저 같은 곳을 예로 들면,

포지션별로 공고가 나가고, 거기에 일할 마음이 있으면 지원하면 됩니다.

https://www.pfizer.com/about/careers/job/4932619?langcode=en Job Details Page | Pfizer

[한국화이자제약] Senior Medical Reviewer (1Year Fixed Term) Korea, Republic of - Seoul Full time Posted 3 Days Ago 4932619 Apply Now Our Purpose We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place. Explore our mission Our Value...

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마침 한국에 리뷰어 자리가 있네요. 1년 계약직. 이런거 많이 해서 경력을 쌓고 다른 회사로 이동하는게 캐나다 식 취업 방법 입니다.

ROLE RESPONSIBILITIES

Serves as the subject matter expert for adherence of promotional and medical content with local laws and industry codes as applicable.

Reviews materials in compliance with applicable SOPs and work instructions.

Ensures the scientific claim is fully substantiated by the cited references.

Meaningfully contribute to cross-functional teams in:

the development of promotional materials at various stages of development

formulating the response to any code complaints or formulation of complaints against competitors

the development brand plans and PoA meetings as appropriate

Serves as a principal contact for audit and inspection teams in relation to compliance of promotional materials and medical content with applicable regulations, codes and company policies. Provides input into development of relevant policies, SOPs and Work Instructions.

Actively contribute to new innovative solutions to improve scientific content review and approval process and to resolve problems based on comprehensive business & scientific knowledge

Actively participates or leads/co-leads local and/or global projects that have an impact beyond the function and/or the country

Contribute to mentoring, coaching and training of new and existing colleagues within the team.

Contribute to resolving issues related to the day-to-day work, proposes recommendations and drives implementation of required changes, new processes, etc.

Contribute to strategic partnerships with relevant cross-functional teams with a view to sustaining, and identifying new ways for Medical to add value to the Pfizer business

QUALIFICATIONS

Technical:

Major in medicine, pharmacy or science with an appropriate life science major preferred. Degrees from other relevant disciplines also considered.

More than 2 years’ experience in the pharmaceutical industry in a Medical Information, Medical Affairs or related function.

Well versed in reviewing promotional materials and medical content & the promotional complaints process.

Demonstrates excellent collaboration, interpersonal & relationship management skills with ability to influence and negotiate outcomes. Experience working in cross-functional teams highly preferred

Ability to work in a virtual work environment

Proficient at critically evaluating literature and writing/summarizing clinical and scientific data

Exhibits strong analytical, oral and written communication skills

Able to work in a fast-paced environment with competing priorities and tight deadlines

Effectively deals with ambiguity and adapts quickly to change

Demonstrates initiative and works independently on complex projects

Fluency in English preferred

Education:

Major in medicine, pharmacy or science with an appropriate life science major preferred. Degrees from other relevant disciplines also considered.

Experience:

More than 2 years’ experience in the pharmaceutical industry in a Medical Information, Medical Affairs or related function.

Work Location Assignment: On Premise